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BiferaRx
BiferaRx - 68220-085-90 - (FOLIC ACID, Heme Iron Polypeptide, IRON DEXTRAN, and CYANOCOBALAMIN)
Drug Information of BiferaRx
| Product NDC: | 68220-085 |
| Proprietary Name: | BiferaRx |
| Non Proprietary Name: | FOLIC ACID, Heme Iron Polypeptide, IRON DEXTRAN, and CYANOCOBALAMIN |
| Active Ingredient(s): | 25; 1; 6; 22 ug/1; mg/1; mg/1; mg/1 & nbsp; FOLIC ACID, Heme Iron Polypeptide, IRON DEXTRAN, and CYANOCOBALAMIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BiferaRx
| Product NDC: | 68220-085 |
| Labeler Name: | Alaven Pharmaceutical LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100501 |
Package Information of BiferaRx
| Package NDC: | 68220-085-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (68220-085-90) |
NDC Information of BiferaRx
| NDC Code | 68220-085-90 |
| Proprietary Name | BiferaRx |
| Package Description | 90 TABLET in 1 BOTTLE (68220-085-90) |
| Product NDC | 68220-085 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FOLIC ACID, Heme Iron Polypeptide, IRON DEXTRAN, and CYANOCOBALAMIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Alaven Pharmaceutical LLC |
| Substance Name | CYANOCOBALAMIN; FOLIC ACID; HEME IRON POLYPEPTIDE; IRON DEXTRAN |
| Strength Number | 25; 1; 6; 22 |
| Strength Unit | ug/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |
