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Trinatal GT
Trinatal GT - 13811-614-90 - (Iron, Biotin, Pantothenic Acid, Calcium Carbonate, Cupric Oxide, Zinc Oxide, Folic Acid, Beta Carotene, Cholecalciferol, .Alpha.-Tocopherol Acetate, DL-, Ascorbic Acid, Thiamine Mononitrate, Riboflavi)
Drug Information of Trinatal GT
| Product NDC: | 13811-614 |
| Proprietary Name: | Trinatal GT |
| Non Proprietary Name: | Iron, Biotin, Pantothenic Acid, Calcium Carbonate, Cupric Oxide, Zinc Oxide, Folic Acid, Beta Carotene, Cholecalciferol, .Alpha.-Tocopherol Acetate, DL-, Ascorbic Acid, Thiamine Mononitrate, Riboflavi |
| Active Ingredient(s): | 10; 120; 2700; 30; 200; 400; 2; 12; 50; 1; 90; 30; 20; 6; 20; 3.4; 3; 15 [iU]/1; mg/1; [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; mg/1 & nbsp; Iron, Biotin, Pantothenic Acid, Calcium Carbonate, Cupric Oxide, Zinc Oxide, Folic Acid, Beta Carotene, Cholecalciferol, .Alpha.-Tocopherol Acetate, DL-, Ascorbic Acid, Thiamine Mononitrate, Riboflavi |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trinatal GT
| Product NDC: | 13811-614 |
| Labeler Name: | TRIGEN Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110705 |
Package Information of Trinatal GT
| Package NDC: | 13811-614-90 |
| Package Description: | 9 BLISTER PACK in 1 CARTON (13811-614-90) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Trinatal GT
| NDC Code | 13811-614-90 |
| Proprietary Name | Trinatal GT |
| Package Description | 9 BLISTER PACK in 1 CARTON (13811-614-90) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 13811-614 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Iron, Biotin, Pantothenic Acid, Calcium Carbonate, Cupric Oxide, Zinc Oxide, Folic Acid, Beta Carotene, Cholecalciferol, .Alpha.-Tocopherol Acetate, DL-, Ascorbic Acid, Thiamine Mononitrate, Riboflavi |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110705 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | TRIGEN Laboratories, Inc. |
| Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; BETA CAROTENE; BIOTIN; CALCIUM CARBONATE; CHOLECALCIFEROL; CUPRIC OXIDE; CYANOCOBALAMIN; DOCUSATE SODIUM; FOLIC ACID; IRON; MAGNESIUM OXIDE; NIACINAMIDE; PANTOTHENIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; ZINC OXIDE |
| Strength Number | 10; 120; 2700; 30; 200; 400; 2; 12; 50; 1; 90; 30; 20; 6; 20; 3.4; 3; 15 |
| Strength Unit | [iU]/1; mg/1; [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; 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] |
