Vitafol-OB Plus DHA
Vitafol -OB+DHA
Approved
Approval ID
a0e273e2-0876-4830-a903-282085be7f32
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 31, 2022
Manufacturers
FDA
Exeltis USA, Inc
DUNS: 071170534
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Vitamin A, Ascorbic Acid, Vitamin D, .Alpha.-Tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, Iron, Magnesium, Zinc, Copper, and Doconexent
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0642-0076
Product Classification
G
Generic Name
Vitamin A, Ascorbic Acid, Vitamin D, .Alpha.-Tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, Iron, Magnesium, Zinc, Copper, and Doconexent
Product Specifications
Effective DateDecember 31, 2022
FDA Product Classification