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V-Natal
V-Natal - 76439-226-90 - (Folic Acid, pyridoxine, Calcium formate, Calcium carbonate, sodium ascorbate, cholecalciferol, acetate ion, thiamine mononitrate, riboflavin, niacinamide, cyanocobalamin, ferrous bisglycinate, potassium iodide, zinc oxide, and choline bitartrate)
Drug Information of V-Natal
| Product NDC: | 76439-226 |
| Proprietary Name: | V-Natal |
| Non Proprietary Name: | Folic Acid, pyridoxine, Calcium formate, Calcium carbonate, sodium ascorbate, cholecalciferol, acetate ion, thiamine mononitrate, riboflavin, niacinamide, cyanocobalamin, ferrous bisglycinate, potassium iodide, zinc oxide, and choline bitartrate |
| Active Ingredient(s): | 30; 45; 155; 450; 55; 10; 32; 1000; 20; 100; 50; 3; 120; 3; 10 [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; Folic Acid, pyridoxine, Calcium formate, Calcium carbonate, sodium ascorbate, cholecalciferol, acetate ion, thiamine mononitrate, riboflavin, niacinamide, cyanocobalamin, ferrous bisglycinate, potassium iodide, zinc oxide, and choline bitartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of V-Natal
| Product NDC: | 76439-226 |
| Labeler Name: | Virtus Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120712 |
Package Information of V-Natal
| Package NDC: | 76439-226-90 |
| Package Description: | 90 TABLET, COATED in 1 BOTTLE (76439-226-90) |
NDC Information of V-Natal
| NDC Code | 76439-226-90 |
| Proprietary Name | V-Natal |
| Package Description | 90 TABLET, COATED in 1 BOTTLE (76439-226-90) |
| Product NDC | 76439-226 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Folic Acid, pyridoxine, Calcium formate, Calcium carbonate, sodium ascorbate, cholecalciferol, acetate ion, thiamine mononitrate, riboflavin, niacinamide, cyanocobalamin, ferrous bisglycinate, potassium iodide, zinc oxide, and choline bitartrate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120712 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Virtus Pharmaceuticals |
| Substance Name | ACETATE ION; CALCIUM CARBONATE; CALCIUM FORMATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CYANOCOBALAMIN; FERROUS BISGLYCINATE; FOLIC ACID; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC OXIDE |
| Strength Number | 30; 45; 155; 450; 55; 10; 32; 1000; 20; 100; 50; 3; 120; 3; 10 |
| Strength Unit | [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |
