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) |
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 NDC: | 68220-085-25 |
Package Description: | 1 BLISTER PACK in 1 CARTON (68220-085-25) > 5 TABLET in 1 BLISTER PACK (68220-085-05) |
NDC Code | 68220-085-25 |
Proprietary Name | BiferaRx |
Package Description | 1 BLISTER PACK in 1 CARTON (68220-085-25) > 5 TABLET in 1 BLISTER PACK (68220-085-05) |
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] |