Tandem – F (US Pharmaceutical Corporation)
Welcome to the PulseAid listing for the Tandem – F 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 and Folic Acid |
SUBSTANCE NAME: | FERROUS ASPARTO GLYCINATE; FOLIC ACID; FERROUS FUMARATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2006-06-17 |
END MARKETING DATE: | 0000-00-00 |
Tandem – F HUMAN PRESCRIPTION DRUG Details:
Item Description | Tandem – F from US Pharmaceutical Corporation |
LABELER NAME: | US Pharmaceutical Corporation |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 115.2; 1; 162(mg/1; mg/1; mg/1) |
START MARKETING DATE: | 2006-06-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52747-901_6f3280b9-49e3-4ff2-9c07-80bd1fded4e4 |
PRODUCT NDC: | 52747-901 |
APPLICATION NUMBER: | |
Other FERROUS ASPARTO GLYCINATE; FOLIC ACID; FERROUS FUMARATE Pharmaceutical Manufacturers / Labelers: