M.V.I. ADULT- retinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, dexpanthenol, biotin, folic acid, and cyanocobalamin kit

M.V.I. Adult by

Drug Labeling and Warnings

M.V.I. Adult by is a Prescription medication manufactured, distributed, or labeled by Hospira, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    M.V.I. Adult™ is a combination of vitamins indicated for the prevention of vitamin deficiency in adults and pediatric patients aged 11 and older receiving parenteral nutrition.

    The physician should not await the development of clinical signs of vitamin deficiency before initiating vitamin therapy.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Dosage and Administration Instructions

    M.V.I. Adult is a combination product that contains the following vitamins: ascorbic acid, vitamin A, vitamin D, thiamine, riboflavin, pyridoxine, niacinamide, dexpanthenol, vitamin E, vitamin K, folic acid, biotin, and vitamin B12.

    M.V.I. Adult is supplied as a single dose or as a pharmacy bulk package for intravenous use intended for administration by intravenous infusion after dilution:

    • M.V.I. Adult Single Dose: consists of two vials which must be mixed prior to use. The mixed solution will provide a single 10 mL dose which must be diluted prior to intravenous administration [see Dosage and Administration (2.3)].
    • M.V.I. Adult Pharmacy Bulk Package: consists of two pharmacy bulk vials which must be mixed prior to use. The mixed solution will provide ten 10 mL single doses which must be diluted prior to intravenous administration. Pharmacy bulk package of M.V.I. Adult is intended for dispensing of single doses to multiple patients in a pharmacy admixture program and is restricted to the preparation of admixtures for infusion [see Dosage and Administration (2.3)].

    Do not administer M.V.I. Adult as a direct, undiluted intravenous injection as it may cause dizziness, faintness, and tissue irritation.

    2.2 Dosage Information

    The recommended daily dosage volume is 10 mL. One daily dose (10 mL) is diluted by adding directly to a specified volume of an intravenous fluid [see Dosage and Administration (2.3)].

    Patients with multiple vitamin deficiencies or with increased vitamin requirements may need multiple daily dosages as indicated or additional doses of individual vitamins.

    2.3 Preparation and Administration Instructions

    M.V.I. Adult supplied as a single dose:

    • M.V.I Adult is to be used only in a suitable work area such as a laminar flow hood (or an equivalent clean air compounding area).
    • Transfer the contents of Vial 1 (5 mL of solution) into the contents of Vial 2 (5 mL of solution). The mixed solution (10 mL) will provide a single 10 mL dose.
    • Once the closure system has been penetrated, complete withdrawal of vial contents within 4 hours. Mixed solution may be stored for up to 4 hours refrigerated.
    • Visually inspect for particulate matter and discoloration prior to intravenous administration.
    • Utilizing a suitable sterile automated compounding device or dispensing pin for accuracy, aseptically transfer the 10 mL dose into a plastic or glass bottle containing at least 500 to 1,000 mL intravenous parenteral nutrition solution containing dextrose or saline.
    • After M.V.I. Adult is diluted in an intravenous infusion, refrigerate the resulting solution unless it is to be used immediately, and use the solution within 24 hours after dilution.
    • Minimize exposure to light because some of the vitamins in M.V.I. Adult, particularly A, D and riboflavin, are light sensitive.

    M.V.I. Adult supplied as a pharmacy bulk package:

    • M.V.I. Adult is to be used only in a suitable work area such as a laminar flow hood (or an equivalent clean air compounding area).
    • Transfer the contents of Vial 1 (50 mL) into Vial 2 (50 mL). The mixed solution (100 mL) will provide ten 10 mL single doses to patients in a pharmacy admixture program.
    • Each bulk vial closure shall be penetrated only one time with a suitable sterile transfer device or dispensing set that allows measured dispensing of the contents.
    • Once the closure system has been penetrated, complete dispensing from the pharmacy bulk vial within 4 hours. Mixed solution may be stored for up to 4 hours refrigerated.
    • Discard unused portion.
    • Visually inspect for particulate matter and discoloration prior to administration.
    • Utilizing a suitable sterile automated compounding device or dispensing pin for accuracy, aseptically transfer each 10 mL dose into a plastic or glass bottle containing at least 500 to 1,000 mL intravenous parenteral nutrition solution containing dextrose or saline.
    • After M.V.I. Adult is diluted in an intravenous infusion, refrigerate the resulting solution unless it is to be used immediately, and use the solution within 24 hours after dilution.
    • Minimize exposure to light because some of the vitamins in M.V.I. Adult, particularly A, D and riboflavin, are light sensitive.

    2.4 Monitoring Vitamin Blood Levels

    Blood vitamin concentrations should be monitored to ensure maintenance of adequate levels, particularly in patients receiving parenteral multivitamins as the only source of vitamins for long periods of time.

    2.5 Drug Incompatibilities

    • M.V.I. Adult is not physically compatible with moderately alkaline solutions such as a sodium bicarbonate solution and other alkaline drugs such as acetazolamide sodium, aminophylline, ampicillin sodium, and chlorothiazide sodium.
    • Folic acid is unstable in the presence of calcium salts such as calcium gluconate.
    • Vitamin A and thiamine in M.V.I.Adult may react with bisulfite solutions such as sodium bisulfite or vitamin K bisulfite. Do not add M.V.I. Adult directly to intravenous fat emulsions.
    • Consult appropriate references for listings of physical and chemical compatibility of solutions and drugs with M.V.I. Adult. In such circumstances, admixture or Y-site administration with M.V.I. Adult should be avoided.
  • 3 DOSAGE FORMS AND STRENGTHS

    M.V.I. Adult is an injection available as a:

    • Single dose: consisting of two vials labeled Vial 1 and Vial 2. Vial 1 is an amber vial containing a clear, amber to orange colored solution. Vial 2 is an amber vial containing a clear to light straw colored solution. Both vials must be mixed prior to use. The mixed solution (10 mL) will provide a single 10 mL dose [see Dosage and Administration (2.3) and Description (11)].
    • Pharmacy bulk package: consisting of two vials labeled Vial 1 and Vial 2. Vial 1 is an amber vial containing a clear, amber to orange colored solution. Vial 2 is an amber vial containing a clear to light straw colored solution. Both vials must be mixed prior to use. The mixed solution (100 mL) will provide ten 10 mL single doses [see Dosage and Administration (2.3))].

    See Description section for vitamin strengths [see Description (11)].

  • 4 CONTRAINDICATIONS

    M.V.I. Adult is contraindicated in patients who have:

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Decreased Anticoagulant Effect of Warfarin

    M.V.I. Adult contains Vitamin K which may decrease the anticoagulant effect of warfarin. In patients who are on warfarin anticoagulant therapy receiving M.V.I. Adult, prothrombin time/INR should be periodically monitored to determine if the dose of warfarin needs to be adjusted.

    5.2 Aluminum Toxicity

    M.V.I. Adult contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration in patients with renal impairment. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.

    Patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 micrograms per kg per day, accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration. To prevent aluminum toxicity monitor periodically aluminum levels with prolonged parenteral administration of M.V.I. Adult.

    5.3 Risk of Low Vitamin A Levels

    Vitamin A may adhere to plastic, resulting in lower vitamin A concentrations after administration of M.V.I. Adult. Therefore, blood vitamin concentrations should be periodically monitored and the administration of additional therapeutic doses of Vitamin A may be required.

    5.4 Allergic Reactions to Thiamine

    Allergic reactions such as urticaria, periorbital and digital edema, have been reported following intravenous administration of thiamine, which is found in M.V.I. Adult. There have been rare reports of anaphylaxis following intravenous doses of thiamine. No fatal anaphylaxis reactions associated with M.V.I. Adult have been reported.

    5.5 Hypervitaminosis A

    Hypervitaminosis A, manifested by nausea, vomiting, headache, dizziness, blurred vision, has been reported in patients with renal failure receiving 1.5 mg/day retinol and in patients with liver disease. Therefore, supplementation of renal failure patients and patients with liver diseases with vitamin A, an ingredient found in M.V.I. Adult, should be undertaken with caution [see Use in Specific Populations (8.6, 8.7)]. Blood levels of Vitamin A should be monitored periodically.

    5.6 Interference with Diagnosis of Megaloblastic Anemia

    M.V.I. Adult contains folic acid and cyanocobalamin which can mask serum deficits of folic acid and cyanocobalamin in patients with megaloblastic anemia. Avoid the use of M.V.I. Adult in patients with suspected or diagnosed megaloblastic anemia prior to blood sampling for the detection of the folic acid and cyanocobalamin deficiencies.

    5.7 Potential to Develop Vitamin Deficiencies or Excesses

    In patients receiving parenteral multivitamins, such as with M.V.I. Adult, blood vitamin concentrations should be periodically monitored to determine if vitamin deficiencies or excesses are developing. M.V.I. Adult may not correct long-standing specific vitamin deficiencies. The administration of additional doses of specific vitamins may be required [see Dosage and Administration (2.2)].

    5.8 Interference with Urine Glucose Testing

    M.V.I. Adult contains Vitamin C which is also known as ascorbic acid. Ascorbic acid in the urine may cause false negative urine glucose determinations.

  • 6 ADVERSE REACTIONS

    The following adverse reactions are discussed in greater detail in other section of the labeling.

    The following adverse reactions have been identified during post approval use of M.V.I. Adult. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Dermatologic: rash, erythema, pruritus
    CNS: headache, dizziness, agitation, anxiety
    Ophthalmic: diplopia

  • 7 DRUG INTERACTIONS

    7.1 Effect of M.V.I. Adult on Other Drugs

    Phenytoin: Folic acid may increase phenytoin metabolism and lower the serum concentration of phenytoin resulting in increased seizure activity.

    Methotrexate: Folic acid may decrease a patient's response to methotrexate therapy.

    Levodopa: Pyridoxine may increase the metabolism of levodopa (decrease blood level of levodopa) and decrease its efficacy.

    Antibiotics: Thiamine, riboflavin, pyridoxine, niacinamide, and ascorbic acid decrease antibiotic activities of erythromycin, kanamycin, streptomycin, doxycycline, and lincomycin.

    Bleomycin: Ascorbic acid and riboflavin inactivate bleomycin in vitro, thus the activity of bleomycin may be reduced.

    7.2 Effect of Other Drugs on M.V.I. Adult

    Hydralazine or Isoniazid:

    Concomitant administration of hydralazine or isoniazid may increase pyridoxine requirements.

    Chloramphenicol:

    In patients with pernicious anemia, the hematologic response to vitamin B12 therapy may be inhibited by concomitant administration of chloramphenicol.

    Phenytoin:

    Phenytoin may decrease serum folic acid concentrations.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Pregnancy Category C

    M.V.I. Adult has not been studied in pregnant women. Pregnant women should follow the U.S. recommended daily allowances for pregnancy because their vitamin requirements may exceed those of nonpregnant women. Animal reproduction studies have not been conducted with M.V.I. Adult (multiple vitamins injection) administered by intravenous infusion.

    8.3 Nursing Mothers

    M.V.I. Adult has not been studied in lactating women. Lactating women should follow the U.S. Recommended Daily Allowances for their condition, because their vitamin requirements may exceed those of nonlactating women. Caution should be exercised when M.V.I. Adult is administered to a nursing woman.

    8.4 Pediatric Use

    M.V.I. Adult is indicated for the prevention of vitamin deficiency in pediatric patients aged 11 years and older receiving parenteral nutrition. M.V.I. Adult is not indicated for use in pediatric patients below the age of 11 years.

    8.5 Geriatric Use

    Reported clinical experience has not identified differences in responses between the elderly and younger patients.

    8.6 Renal Impairment

    M.V.I. Adult has not been studied in patients with renal impairment. Monitor renal function, calcium, phosphorus and vitamin A levels in patients with renal impairment [see Warnings and Precautions (5.2, 5.5)].

    8.7 Hepatic Impairment

    M.V.I. Adult has not been studied in patients with hepatic impairment. Monitor vitamin A level in patients with liver disease or high alcohol consumption [see Warnings and Precautions (5.5)].

  • 10 OVERDOSAGE

    Signs and symptoms of acute or chronic overdosage may be those of individual M.V.I. Adult component toxicity. There is no clinical experience with M.V.I. Adult overdosage.

  • 11 DESCRIPTION

    M.V.I. Adult (multiple vitamins injection) is a sterile product consisting of two vials provided as a single dose or as a pharmacy bulk package for intravenous use intended for administration by intravenous infusion after dilution.

    Table 1 provides the strengths of the vitamins provided in vial 1 and vial 2:

    Table 1: M.V.I. ADULT FORMULATION (INTENDED FOR AGES 11 AND OLDER)

    Vial 1*

    Fat Soluble Vitamins**

    Ingredient

    Amount per Unit Dose

    Vitamin A (retinol)

    1 mga

    Vitamin D (ergocalciferol)

    5 mcgb

    Vitamin E (dl-alpha-tocopheryl acetate)

    10 mgc

    Vitamin K (phytonadione)

    150 mcg

    Water Soluble Vitamins

    Vitamin C (ascorbic acid)

    200 mg

    Niacinamide

    40 mg

    Vitamin B2 (as riboflavin 5-phosphate sodium)

    3.6 mg

    Vitamin B1 (thiamine)

    6 mg

    Vitamin B6 (pyridoxine HCl)

    6 mg

    Dexpanthenol (d-pantothenyl alcohol)

    15 mg

    *    With 30% propylene glycol and 2% gentisic acid ethanolamide as stabilizers and preservatives; sodium hydroxide for pH adjustment; 1.6% polysorbate 80; 0.028% polysorbate 20; 0.002% butylated hydroxytoluene; 0.0005% butylated hydroxyanisole.
    **   Fat soluble vitamins A, D, E and K are water solubilized with polysorbate 80.
    (a) 1 mg vitamin A equals 3,300 USP units.
    (b) 5 mcg ergocalciferol equals 200 USP units.
    (c) 10 mg vitamin E equals 10 USP units.

    Vial 2*

    Biotin

    60 mcg

    Folic acid

    600 mcg

    B12 (cyanocobalamin)

    5 mcg

    *      With 30% propylene glycol; and citric acid, sodium citrate, and sodium hydroxide for pH adjustment.

    Multiple vitamin preparation for intravenous infusion:

    M.V.I. Adult (multiple vitamins injection) makes available a combination of fat-soluble and water-soluble vitamins in an aqueous solution, formulated for incorporation into intravenous infusions. The liposoluble vitamins A, D, E, and K have been solubilized in an aqueous medium with polysorbate 80, permitting intravenous administration of these vitamins.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenicity, mutagenicity and fertility studies were not performed.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    M.V.I. ADULT is an injection supplied in the following package configurations:

    M.V.I. ADULT Single-Dose

    Unit of Sale

    Each Box

    Each

    Vial 1

    Each

    Vial 2

    NDC: 61703-434-82

    Bundle of 10 Boxes of
    2 vials (Vial 1 and
    Vial 2)

    NDC: 61703-434-01

    Box of 2 vials
    (Vial 1 and Vial 2)

    NDC: 61703-426-02

    10 Vitamin Blend,
    5 mL

    NDC: 61703-430-02

    3 Vitamin Blend,
    5 mL

    Vial 1 is an amber vial containing a clear, amber to orange colored solution. Vial 2 is an amber vial containing a clear to light straw colored solution. Mix contents of Vial 1 and Vial 2 to provide a single 10 mL dose [see Dosage and Administration (2.3)].

    M.V.I. ADULT Pharmacy Bulk Package

    Unit of Sale

    Intermediate

    Multi-Pack

    Each

    Vial 1

    Each

    Vial 2

    NDC: 61703-422-83

    Case of 2 Boxes of
    10 vials (5 Vial 1 and
    5 Vial 2)

    NDC: 61703-422-78

    Box of 10 vials
    (5 Vial 1 and 5 Vial 2)

    NDC: 61703-426-01

    10 Vitamin Blend,
    50 mL

    NDC: 61703-430-01

    3 Vitamin Blend,
    50 mL

    Vial 1 is an amber vial containing a clear, amber to orange colored solution. Vial 2 is an amber vial containing a clear to light straw colored solution. Mix contents of Vial 1 and Vial 2 to provide ten 10 mL single doses [see Dosage and Administration (2.3)].

    See Description section for vitamin strengths [see Description (11)].

    Minimize the exposure of M.V.I. Adult to light, because vitamins A, D and riboflavin are light sensitive.

    Store at 2-8°C (36-46°F).

  • 17 PATIENT COUNSELING INFORMATION

    Instruct patients (if age appropriate) and caregivers:

    • To watch for and immediately report signs of allergic reactions (i.e. urticaria, periorbital and digital edema).
    • To watch for and immediately report signs of hypervitaminosis A, manifested by nausea, vomiting, headache, dizziness, blurred vision, if patients have renal impairment.
    • To report other adverse reactions such as rash, erythema, pruritus, headache, dizziness, agitation, anxiety, and diplopia.
    • That patients on warfarin anticoagulant therapy will be monitored periodically for blood prothrombin/ INR levels to determine if the dose of warfarin needs to be adjusted.
    • About the significance of periodic monitoring of blood vitamin concentrations to determine if vitamin deficiencies or excesses are developing .
    • About the need to monitor renal function, calcium, phosphorus, aluminum, and vitamin A levels in patients with renal impairment.

     

    Manufactured by                                                                                                                        Hospira logo
    Hospira, Inc., Lake Forest, IL 60045 USA

    LAB-0989-2.0

  • PRINCIPAL DISPLAY PANEL - Kit Carton - NDC: 61703-422-78

    Sterile
    Contents: 10 vials, 50 mL Fill each
    (5 Vial 1 and 5 Vial 2)
    Mix contents of Vial 1 with Vial 2 to provide 10 single doses.

    NDC: 61703-422-78

    Rx only

    M.V.I. ADULT™
    (multiple vitamins injection)

    PHARMACY BULK PACKAGE. NOT FOR DIRECT INFUSION.

    See insert for important information on pharmacy bulk package.

    Store under refrigeration, 2 - 8°C (36 - 46°F). Store Upright.

    Hospira

    PRINCIPAL DISPLAY PANEL - Kit Carton - NDC: <a href=/NDC/61703-422-78>61703-422-78</a>
  • PRINCIPAL DISPLAY PANEL - 50 mL Vial Label - NDC: 61703-426-01

    M.V.I. ADULT™
    (multiple vitamins injection)

    PHARMACY BULK PACKAGE. NOT FOR DIRECT INFUSION.

    Vial 1
    Rx only

    50 mL Multiple Dose Vial, Sterile

    See insert for important information on pharmacy bulk
    package.

    Store under refrigeration, 2-8°C (36-46°F).

    PRINCIPAL DISPLAY PANEL - 50 mL Vial Label - NDC: <a href=/NDC/61703-426-01>61703-426-01</a>
  • PRINCIPAL DISPLAY PANEL - 50 mL Vial Label - NDC: 61703-430-01

    LIFT
    HERE

    NDC: 61703-430-01

    M.V.I.-ADULT™
    (multiple vitamins injection)

    PHARMACY BULK PACKAGE.
    NOT FOR DIRECT INFUSION.

    Vial 2
    Rx only

    50 mL Fill Multiple Dose Vial, Sterile

    See insert for important information
    on pharmacy bulk package.

    Store under refrigeration, 2-8°C (36-46°F).

    Hospira, Inc.
    Lake Forest, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 50 mL Vial Label - NDC: <a href=/NDC/61703-430-01>61703-430-01</a>
  • PRINCIPAL DISPLAY PANEL - Kit Carton - NDC: 61703-434-01

    Sterile

    NDC: 61703-434-01
    Rx only

    M.V.I. ADULT™
    (multiple vitamins injection)

    FOR DILUTION IN INTRAVENOUS
    INFUSIONS ONLY.

    Contents: Vial 1 (5 mL) and Vial 2 (5 mL).
    Both vials to be used for a single dose.

    Store under refrigeration, 2 - 8°C (36 - 46°F).

    Store Upright

    Hospira

    PRINCIPAL DISPLAY PANEL - Kit Carton - NDC: <a href=/NDC/61703-434-01>61703-434-01</a>
  • PRINCIPAL DISPLAY PANEL - 5 mL Vial Label - NDC: 61703-426-02

    M.V.I. ADULT™
    (multiple vitamins injection)

    For Intravenous Infusion Only.

    Vial 1
    Rx only

    5 mL Single Dose Vial, Sterile

    Store under refrigeration,
    2 - 8°C (36 - 46°F).

    Hospira, Inc., Lake Forest, IL 60045 USA

    PRINCIPAL DISPLAY PANEL - 5 mL Vial Label - NDC: <a href=/NDC/61703-426-02>61703-426-02</a>
  • PRINCIPAL DISPLAY PANEL - 5 mL Vial Label - NDC: 61703-430-02

    NDC: 61703-430-02

    M.V.I. ADULT™
    (multiple vitamins injection)

    For Intravenous Infusion Only.

    Vial 2
    Rx only

    5 mL Single Dose Vial, Sterile

    Store under refrigeration,
    2 - 8°C (36 - 46°F).

    Hospira, Inc., Lake Forest, IL 60045 USA

    PRINCIPAL DISPLAY PANEL - 5 mL Vial Label - NDC: <a href=/NDC/61703-430-02>61703-430-02</a>
  • INGREDIENTS AND APPEARANCE
    M.V.I. ADULT 
    retinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, dexpanthenol, biotin, folic acid, and cyanocobalamin kit
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 61703-422
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 61703-422-832 in 1 CASE01/27/2015
    1NDC: 61703-422-785 in 1 BOX
    11 in 1 KIT
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 VIAL, MULTI-DOSE 50 mL
    Part 21 VIAL, MULTI-DOSE 50 mL
    Part 1 of 2
    RETINOL, ERGOCALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PHYTONADIONE, ASCORBIC ACID, NIACINAMIDE, RIBOFLAVIN 5-PHOSPHATE SODIUM, THIAMINE HYDROCHLORIDE, PYRIDOXINE HYDROCHLORIDE, AND DEXPANTHENOL 
    retinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, and dexpanthenol injection, solution, concentrate
    Product Information
    Item Code (Source)NDC: 61703-426
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL1 mg  in 5 mL
    ERGOCALCIFEROL (UNII: VS041H42XC) (ERGOCALCIFEROL - UNII:VS041H42XC) ERGOCALCIFEROL5 ug  in 5 mL
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) (.ALPHA.-TOCOPHEROL, DL- - UNII:7QWA1RIO01) .ALPHA.-TOCOPHEROL, DL-10 mg  in 5 mL
    PHYTONADIONE (UNII: A034SE7857) (PHYTONADIONE - UNII:A034SE7857) PHYTONADIONE150 ug  in 5 mL
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID200 mg  in 5 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE40 mg  in 5 mL
    RIBOFLAVIN 5'-PHOSPHATE SODIUM (UNII: 20RD1DZH99) (FLAVIN MONONUCLEOTIDE - UNII:7N464URE7E) FLAVIN MONONUCLEOTIDE3.6 mg  in 5 mL
    THIAMINE HYDROCHLORIDE (UNII: M572600E5P) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE6 mg  in 5 mL
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE HYDROCHLORIDE6 mg  in 5 mL
    DEXPANTHENOL (UNII: 1O6C93RI7Z) (DEXPANTHENOL - UNII:1O6C93RI7Z) DEXPANTHENOL15 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GENTISIC ACID ETHANOLAMIDE (UNII: H4E039OIGX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 61703-426-0150 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02162501/27/2015
    Part 2 of 2
    BIOTIN, FOLIC ACID, AND CYANOCOBALAMIN 
    biotin, folic acid, and cyanocobalamin injection, solution, concentrate
    Product Information
    Item Code (Source)NDC: 61703-430
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN60 ug  in 5 mL
    FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID600 ug  in 5 mL
    CYANOCOBALAMIN (UNII: P6YC3EG204) (CYANOCOBALAMIN - UNII:P6YC3EG204) CYANOCOBALAMIN5 ug  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 61703-430-0150 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02162501/27/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02162501/27/2015
    M.V.I. ADULT 
    retinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, dexpanthenol, biotin, folic acid, and cyanocobalamin kit
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 61703-434
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 61703-434-8210 in 1 PACKAGE04/28/2017
    1NDC: 61703-434-011 in 1 KIT
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 VIAL, SINGLE-DOSE 5 mL
    Part 21 VIAL, SINGLE-DOSE 5 mL
    Part 1 of 2
    RETINOL, ERGOCALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, PHYTONADIONE, ASCORBIC ACID, NIACINAMIDE, RIBOFLAVIN 5-PHOSPHATE SODIUM, THIAMINE HYDROCHLORIDE, PYRIDOXINE HYDROCHLORIDE, AND DEXPANTHENOL 
    retinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, and dexpanthenol injection, solution, concentrate
    Product Information
    Item Code (Source)NDC: 61703-426
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL1 mg  in 5 mL
    ERGOCALCIFEROL (UNII: VS041H42XC) (ERGOCALCIFEROL - UNII:VS041H42XC) ERGOCALCIFEROL5 ug  in 5 mL
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) (.ALPHA.-TOCOPHEROL, DL- - UNII:7QWA1RIO01) .ALPHA.-TOCOPHEROL, DL-10 mg  in 5 mL
    PHYTONADIONE (UNII: A034SE7857) (PHYTONADIONE - UNII:A034SE7857) PHYTONADIONE150 ug  in 5 mL
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID200 mg  in 5 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE40 mg  in 5 mL
    RIBOFLAVIN 5'-PHOSPHATE SODIUM (UNII: 20RD1DZH99) (FLAVIN MONONUCLEOTIDE - UNII:7N464URE7E) FLAVIN MONONUCLEOTIDE3.6 mg  in 5 mL
    THIAMINE HYDROCHLORIDE (UNII: M572600E5P) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE6 mg  in 5 mL
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE HYDROCHLORIDE6 mg  in 5 mL
    DEXPANTHENOL (UNII: 1O6C93RI7Z) (DEXPANTHENOL - UNII:1O6C93RI7Z) DEXPANTHENOL15 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GENTISIC ACID ETHANOLAMIDE (UNII: H4E039OIGX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 61703-426-025 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02162504/28/2017
    Part 2 of 2
    BIOTIN, FOLIC ACID, AND CYANOCOBALAMIN 
    biotin, folic acid, and cyanocobalamin injection, solution, concentrate
    Product Information
    Item Code (Source)NDC: 61703-430
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN60 ug  in 5 mL
    FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID600 ug  in 5 mL
    CYANOCOBALAMIN (UNII: P6YC3EG204) (CYANOCOBALAMIN - UNII:P6YC3EG204) CYANOCOBALAMIN5 ug  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 61703-430-025 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02162504/28/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02162504/28/2017
    Labeler - Hospira, Inc. (141588017)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hospira, Inc.093132819ANALYSIS(61703-422, 61703-434) , LABEL(61703-422, 61703-434) , MANUFACTURE(61703-422, 61703-434) , PACK(61703-422, 61703-434)

    • Trademark Results [M.V.I. Adult]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    M.V.I. ADULT
    M.V.I. ADULT
    78496648 3045425 Live/Registered
    HOSPIRA, INC.
    2004-10-08
    M.V.I. ADULT
    M.V.I. ADULT
    78207887 not registered Dead/Abandoned
    aaiPharma, LLC
    2003-01-28
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