NDC 0480-7253 is a Tablet, Film Coated in the Bulk Ingredient category. It is labeled and distributed by Teva Pharmaceutical Industries Ltd..
| Product ID | 0480-7253_218bb318-aa2d-45af-b777-00f36c620374 |
| NDC | 0480-7253 |
| Product Type | Bulk Ingredient |
| Proprietary Name | NDC 0480-7253 |
| Dosage Form | Tablet, Film Coated |
| Marketing Start Date | 2005-09-01 |
| Marketing Category | / DRUG FOR FURTHER PROCESSING |
| Labeler Name | Teva Pharmaceutical Industries Ltd. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076447 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-09-17 |
| Marketing End Date | 2013-12-26 |
| Marketing Category | ANDA |
| Application Number | ANDA076447 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-09-17 |
| Marketing End Date | 2013-12-26 |
| Marketing Category | ANDA |
| Application Number | ANDA076447 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-09-17 |
| Marketing End Date | 2013-12-26 |
| Ingredient | Strength |
|---|---|
| FEXOFENADINE HYDROCHLORIDE | 180 mg/1 |