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Prenate Elite
Prenate Elite - 75854-301-30 - (.beta.-carotene, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, biotin, calcium pantothenate, calcium carbonate, ferrous fumarate, potassium iodide, magnesium oxide, zinc oxide and cupric oxide)
Drug Information of Prenate Elite
| Product NDC: | 75854-301 |
| Proprietary Name: | Prenate Elite |
| Non Proprietary Name: | .beta.-carotene, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, biotin, calcium pantothenate, calcium carbonate, ferrous fumarate, potassium iodide, magnesium oxide, zinc oxide and cupric oxide |
| Active Ingredient(s): | 10; 2600; 75; 330; 100; 6; 450; 1.5; 13; 26; 1; 25; 21; 150; 21; 3.5; 3; 15 [iU]/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1 & nbsp; .beta.-carotene, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, biotin, calcium pantothenate, calcium carbonate, ferrous fumarate, potassium iodide, magnesium oxide, zinc oxide and cupric oxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prenate Elite
| Product NDC: | 75854-301 |
| Labeler Name: | Avion Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120806 |
Package Information of Prenate Elite
| Package NDC: | 75854-301-30 |
| Package Description: | 30 TABLET, COATED in 1 BOTTLE (75854-301-30) |
NDC Information of Prenate Elite
| NDC Code | 75854-301-30 |
| Proprietary Name | Prenate Elite |
| Package Description | 30 TABLET, COATED in 1 BOTTLE (75854-301-30) |
| Product NDC | 75854-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | .beta.-carotene, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, biotin, calcium pantothenate, calcium carbonate, ferrous fumarate, potassium iodide, magnesium oxide, zinc oxide and cupric oxide |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120806 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Avion Pharmaceuticals, LLC |
| Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; .BETA.-CAROTENE; ASCORBIC ACID; BIOTIN; CALCIUM CARBONATE; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE; ZINC OXIDE |
| Strength Number | 10; 2600; 75; 330; 100; 6; 450; 1.5; 13; 26; 1; 25; 21; 150; 21; 3.5; 3; 15 |
| Strength Unit | [iU]/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/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],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] |
