Tandem (US Pharmaceutical Corporation)
Welcome to the PulseAid listing for the Tandem drug offered from US Pharmaceutical Corporation. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | US Pharmaceutical Corporation |
| NON-PROPRIETARY NAME: | Ferrous Fumarate and Polysacchride Iron Complex |
| SUBSTANCE NAME: | FERROUS FUMARATE; FERROUS ASPARTO GLYCINATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2006-02-17 |
| END MARKETING DATE: | 0000-00-00 |
Tandem HUMAN PRESCRIPTION DRUG Details:
| Item Description | Tandem from US Pharmaceutical Corporation |
| LABELER NAME: | US Pharmaceutical Corporation |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 162; 115.2(mg/1; mg/1) |
| START MARKETING DATE: | 2006-02-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 52747-900_6f3280b9-49e3-4ff2-9c07-80bd1fded4e4 |
| PRODUCT NDC: | 52747-900 |
| APPLICATION NUMBER: | |
Other FERROUS FUMARATE; FERROUS ASPARTO GLYCINATE Pharmaceutical Manufacturers / Labelers:
