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NDC 00642-0093-03 Vitafol 9; 30; 330; 25; 2; 12; 200; 680; 29; 1020; 20; 15; 150; 2.5; 1.8; 1.6; 25 mg/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1 Details
Vitafol 9; 30; 330; 25; 2; 12; 200; 680; 29; 1020; 20; 15; 150; 2.5; 1.8; 1.6; 25 mg/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1
Vitafol is a ORAL CAPSULE, LIQUID FILLED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Exeltis USA, Inc.. The primary component is .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; BETA CAROTENE; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; DOCONEXENT; FOLIC ACID; IRON; LEVOMEFOLATE CALCIUM; MAGNESIUM OXIDE; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMIN.
Product Information
NDC | 00642-0093 |
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Product ID | 0642-0093_f6df2d91-9721-c396-e053-6394a90a48b0 |
Associated GPIs | 78516058000130 |
GCN Sequence Number | 071399 |
GCN Sequence Number Description | PNV 67/iron ps/folate no.1/dha CAPSULE 29-1-200MG ORAL |
HIC3 | C6F |
HIC3 Description | PRENATAL VITAMIN PREPARATIONS |
GCN | 35169 |
HICL Sequence Number | 040586 |
HICL Sequence Number Description | PRENATAL VIT NO.67/IRON POLYSACCHARIDES/FOLATE COMB.NO.1/DHA |
Brand/Generic | Brand |
Proprietary Name | Vitafol |
Proprietary Name Suffix | Ultra |
Non-Proprietary Name | Doconexent, Niacinamide, .Alpha.-Tocopherol Acetate, DL-, Cholecalciferol, .Beta.-Carotene, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc Oxide, Cupric Oxide, Potassium Iodide, Magnesium Oxide, Folic |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | CAPSULE, LIQUID FILLED |
Route | ORAL |
Active Ingredient Strength | 9; 30; 330; 25; 2; 12; 200; 680; 29; 1020; 20; 15; 150; 2.5; 1.8; 1.6; 25 |
Active Ingredient Units | mg/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1 |
Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; BETA CAROTENE; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; DOCONEXENT; FOLIC ACID; IRON; LEVOMEFOLATE CALCIUM; MAGNESIUM OXIDE; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMIN |
Labeler Name | Exeltis USA, Inc. |
Pharmaceutical Class | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Calculi Dissolution Agent [EPC], Folate Analog [EPC], Folic Acid [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED DRUG OTHER |
Application Number | n/a |
Listing Certified Through | 2024-12-31 |
Package
NDC 00642-0093-03 (00642009303)
NDC Package Code | 0642-0093-03 |
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Billing NDC | 00642009303 |
Package | 1 BLISTER PACK in 1 BOX (0642-0093-03) / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Marketing Start Date | 2013-09-23 |
NDC Exclude Flag | N |
Pricing Information | N/A |