NDC 61703-422

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

M.V.I. Adult is a Kit in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is .

Product ID61703-422_16db3dcb-55d6-4554-aeb0-f62c97838244
NDC61703-422
Product TypeHuman Prescription Drug
Proprietary NameM.V.I. Adult
Generic NameRetinol, Ergocalciferol, .alpha.-tocopherol Acetate, Dl-, Phytonadione, Ascorbic Acid, Niacinamide, Riboflavin 5-phosphate Sodium, Thiamine Hydrochloride, Pyridoxine Hydrochloride, Dexpanthenol, Biotin, Folic Acid, And Cyanocobalamin
Dosage FormKit
Marketing Start Date2015-01-27
Marketing CategoryNDA / NDA
Application NumberNDA021625
Labeler NameHospira, Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 61703-422-83

2 BOX in 1 CASE (61703-422-83) > 5 KIT in 1 BOX (61703-422-78) > 1 KIT in 1 KIT * 50 mL in 1 VIAL, MULTI-DOSE (61703-426-01) * 50 mL in 1 VIAL, MULTI-DOSE (61703-430-01)
Marketing Start Date2015-01-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61703-422-81 [61703042281]

M.V.I. Adult KIT
Marketing CategoryNDA
Application NumberNDA021625
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2004-07-15
Marketing End Date2012-02-13

NDC 61703-422-78 [61703042278]

M.V.I. Adult KIT
Marketing CategoryNDA
Application NumberNDA021625
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-01-28

NDC 61703-422-82 [61703042282]

M.V.I. Adult KIT
Marketing CategoryNDA
Application NumberNDA021625
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2004-07-15
Marketing End Date2018-05-01

NDC 61703-422-83 [61703042283]

M.V.I. Adult KIT
Marketing CategoryNDA
Application NumberNDA021625
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-01-27

NDC 61703-422-73 [61703042273]

M.V.I. Adult KIT
Marketing CategoryNDA
Application NumberNDA021625
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-01-28
Marketing End Date2015-04-29

Drug Details

OpenFDA Data

SPL SET ID:e3912909-50c7-4ad2-49b5-ae3a3dfec758
Manufacturer

NDC Crossover Matching brand name "M.V.I. Adult" or generic name "Retinol, Ergocalciferol, .alpha.-tocopherol Acetate, Dl-, Phytonadione, Ascorbic Acid, Niacinamide, Riboflavin 5-phosphate Sodium, Thiamine Hydrochloride, Pyridoxine Hydrochloride, Dexpanthenol, Biotin, Folic Acid, And Cyanocobalamin"

NDCBrand NameGeneric Name
61703-422M.V.I. Adultretinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, dexpanthenol, biotin, folic acid, and cyanocobalamin
61703-434M.V.I. Adultretinol, ergocalciferol, .alpha.-tocopherol acetate, dl-, phytonadione, ascorbic acid, niacinamide, riboflavin 5-phosphate sodium, thiamine hydrochloride, pyridoxine hydrochloride, dexpanthenol, biotin, folic acid, and cyanocobalamin

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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