NDC 0642-0204

Strovite Forte Caplet

Vitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Biotin, Pantothenic Acid, Magnesium, Zinc, Selenium, Copper, Chromium, Molybdenum, And Iron

Strovite Forte Caplet is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Everett Laboratories, Inc.. The primary component is Vitamin A; Ascorbic Acid; Vitamin D; .alpha.-tocopherol; Thiamine Mononitrate; Riboflavin; Niacin; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Biotin; Pantothenic Acid; Magnesium; Zinc; Selenium; Copper; Chromium; Molybdenum; Iron.

Product ID0642-0204_13d4ddf2-f701-441b-87d6-010bc26f677d
NDC0642-0204
Product TypeHuman Prescription Drug
Proprietary NameStrovite Forte Caplet
Generic NameVitamin A, Ascorbic Acid, Vitamin D, .alpha.-tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Biotin, Pantothenic Acid, Magnesium, Zinc, Selenium, Copper, Chromium, Molybdenum, And Iron
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date1996-10-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameEverett Laboratories, Inc.
Substance NameVITAMIN A; ASCORBIC ACID; VITAMIN D; .ALPHA.-TOCOPHEROL; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; PANTOTHENIC ACID; MAGNESIUM; ZINC; SELENIUM; COPPER; CHROMIUM; MOLYBDENUM; IRON
Active Ingredient Strength4000 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1
Pharm ClassesVitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE],Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 0642-0204-10

100 TABLET, COATED in 1 BOTTLE (0642-0204-10)
Marketing Start Date1996-10-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0642-0204-10 [00642020410]

Strovite Forte Caplet TABLET, COATED
Marketing CategoryUNAPPROVED DRUG OTHER
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-10-01
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
VITAMIN A4000 [iU]/1

OpenFDA Data

SPL SET ID:add96910-9404-48aa-bb3c-945e321a11ab
Manufacturer
UNII
UPC Code
  • 0306420204104
  • Pharmacological Class

    • Vitamin A [CS]
    • Vitamin A [EPC]
    • Vitamin C [EPC]
    • Ascorbic Acid [CS]
    • Vitamin D [CS]
    • Vitamin D [EPC]
    • Nicotinic Acid [EPC]
    • Nicotinic Acids [CS]
    • Vitamin B6 Analog [EPC]
    • Vitamin B 6 [Chemical/Ingredient]
    • Analogs/Derivatives [Chemical/Ingredient]
    • Vitamin B 12 [CS]
    • Vitamin B12 [EPC]
    • Copper [CS]
    • Copper-containing Intrauterine Device [EPC]
    • Decreased Embryonic Implantation [PE]
    • Decreased Sperm Motility [PE]
    • Inhibit Ovum Fertilization [PE]
    • Standardized Chemical Allergen [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Allergens [CS]

    Trademark Results [Strovite Forte]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    STROVITE FORTE
    STROVITE FORTE
    76025557 2455180 Live/Registered
    EXELTIS USA, INC.
    2000-04-13

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.