| Product NDC: | 52747-901 |
| Proprietary Name: | Tandem - F |
| Non Proprietary Name: | Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid |
| Active Ingredient(s): | 115.2; 162; 1 mg/1; mg/1; mg/1 & nbsp; Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52747-901 |
| Labeler Name: | US Pharmaceutical Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20060617 |
| Package NDC: | 52747-901-60 |
| Package Description: | 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-901-60) |
| NDC Code | 52747-901-60 |
| Proprietary Name | Tandem - F |
| Package Description | 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-901-60) |
| Product NDC | 52747-901 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20060617 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | US Pharmaceutical Corporation |
| Substance Name | FERROUS ASPARTO GLYCINATE; FERROUS FUMARATE; FOLIC ACID |
| Strength Number | 115.2; 162; 1 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |