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TRICARE PRENATAL
TRICARE PRENATAL - 67112-101-00 - (ASCORBIC ACID, CHOLECALCIFEROL, DL-.ALPHA.-TOCOPHEROL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM CARBONATE, FERROUS FUMARAT)
Drug Information of TRICARE PRENATAL
| Product NDC: | 67112-101 |
| Proprietary Name: | TRICARE PRENATAL |
| Non Proprietary Name: | ASCORBIC ACID, CHOLECALCIFEROL, DL-.ALPHA.-TOCOPHEROL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM CARBONATE, FERROUS FUMARAT |
| Active Ingredient(s): | 30; 100; 200; 400; 2; 12; 27; 1; 20; 3.1; 1.6; 1.6; 10 [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; ASCORBIC ACID, CHOLECALCIFEROL, DL-.ALPHA.-TOCOPHEROL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM CARBONATE, FERROUS FUMARAT |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRICARE PRENATAL
| Product NDC: | 67112-101 |
| Labeler Name: | Medecor Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20021111 |
Package Information of TRICARE PRENATAL
| Package NDC: | 67112-101-00 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (67112-101-00) |
NDC Information of TRICARE PRENATAL
| NDC Code | 67112-101-00 |
| Proprietary Name | TRICARE PRENATAL |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (67112-101-00) |
| Product NDC | 67112-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ASCORBIC ACID, CHOLECALCIFEROL, DL-.ALPHA.-TOCOPHEROL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM CARBONATE, FERROUS FUMARAT |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20021111 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Medecor Pharma, LLC |
| Substance Name | .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; ZINC OXIDE |
| Strength Number | 30; 100; 200; 400; 2; 12; 27; 1; 20; 3.1; 1.6; 1.6; 10 |
| Strength Unit | [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/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],Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE] |
