Product NDC: | 0178-0716 |
Proprietary Name: | NataFort |
Non Proprietary Name: | Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, and Iron |
Active Ingredient(s): | 11; 120; 400; 12; 1; 60; 20; 10; 3; 2 [iU]/1; mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, and Iron |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0178-0716 |
Labeler Name: | Mission Pharmacal Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110825 |
Package NDC: | 0178-0716-90 |
Package Description: | 90 TABLET in 1 BOTTLE (0178-0716-90) |
NDC Code | 0178-0716-90 |
Proprietary Name | NataFort |
Package Description | 90 TABLET in 1 BOTTLE (0178-0716-90) |
Product NDC | 0178-0716 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ascorbic acid, Cholecalciferol, .alpha.-tocopherol acetate, dl-, Thiamine mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, and Iron |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110825 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Mission Pharmacal Company |
Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; FOLIC ACID; IRON; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE |
Strength Number | 11; 120; 400; 12; 1; 60; 20; 10; 3; 2 |
Strength Unit | [iU]/1; mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |