Cefdinir (Teva Pharmaceuticals USA Inc)
Welcome to the PulseAid listing for the Cefdinir drug offered from Teva Pharmaceuticals USA Inc. This Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] 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: | Teva Pharmaceuticals USA Inc |
| NON-PROPRIETARY NAME: | Cefdinir |
| SUBSTANCE NAME: | CEFDINIR MONOHYDRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | POWDER, FOR SUSPENSION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2007-05-08 |
| END MARKETING DATE: | 0000-00-00 |
Cefdinir HUMAN PRESCRIPTION DRUG Details:
| Item Description | Cefdinir from Teva Pharmaceuticals USA Inc |
| LABELER NAME: | Teva Pharmaceuticals USA Inc |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 125(mg/5mL) |
| START MARKETING DATE: | 2007-05-08 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-4136_51369e23-02c4-4a1b-930c-d81627510b85 |
| PRODUCT NDC: | 0093-4136 |
| APPLICATION NUMBER: | ANDA065332 |
Other CEFDINIR MONOHYDRATE Pharmaceutical Manufacturers / Labelers:
