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Se-Natal One
Se-Natal One - 13925-103-01 - (Vitamin A Acetate, Cholecalciferol, .Alpha.-Tocopherol, Dl, Niacinamide Ascorbate, Folic Acid, Thiamine Hydrochloride, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Cyanocobalamin, Biotin, Pantothenic Acid, Calcium Carbonate, Ferrous Fumarate, Magnesium Oxide, Cupric Oxide and Zinc Oxide)
Drug Information of Se-Natal One
| Product NDC: | 13925-103 |
| Proprietary Name: | Se-Natal One |
| Non Proprietary Name: | Vitamin A Acetate, Cholecalciferol, .Alpha.-Tocopherol, Dl, Niacinamide Ascorbate, Folic Acid, Thiamine Hydrochloride, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Cyanocobalamin, Biotin, Pantothenic Acid, Calcium Carbonate, Ferrous Fumarate, Magnesium Oxide, Cupric Oxide and Zinc Oxide |
| Active Ingredient(s): | 15; 30; 200; 400; 3; 2.5; 60; 1; 100; 17; 80; 7; 4; 1.6; 1.5; 4000; 25 [iU]/1; ug/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; mg/1 & nbsp; Vitamin A Acetate, Cholecalciferol, .Alpha.-Tocopherol, Dl, Niacinamide Ascorbate, Folic Acid, Thiamine Hydrochloride, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Cyanocobalamin, Biotin, Pantothenic Acid, Calcium Carbonate, Ferrous Fumarate, Magnesium Oxide, Cupric Oxide and Zinc Oxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Se-Natal One
| Product NDC: | 13925-103 |
| Labeler Name: | Seton Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090416 |
Package Information of Se-Natal One
| Package NDC: | 13925-103-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (13925-103-01) |
NDC Information of Se-Natal One
| NDC Code | 13925-103-01 |
| Proprietary Name | Se-Natal One |
| Package Description | 100 TABLET in 1 BOTTLE (13925-103-01) |
| Product NDC | 13925-103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Vitamin A Acetate, Cholecalciferol, .Alpha.-Tocopherol, Dl, Niacinamide Ascorbate, Folic Acid, Thiamine Hydrochloride, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Cyanocobalamin, Biotin, Pantothenic Acid, Calcium Carbonate, Ferrous Fumarate, Magnesium Oxide, Cupric Oxide and Zinc Oxide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090416 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Seton Pharmaceuticals |
| Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; BIOTIN; CALCIUM CARBONATE; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; NIACINAMIDE; NIACINAMIDE ASCORBATE; PANTOTHENIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; VITAMIN A ACETATE; ZINC OXIDE |
| Strength Number | 15; 30; 200; 400; 3; 2.5; 60; 1; 100; 17; 80; 7; 4; 1.6; 1.5; 4000; 25 |
| Strength Unit | [iU]/1; ug/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; mg/1 |
| Pharmaceutical Classes | Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |
