NDC 49884-121 is a in the category. It is labeled and distributed by Par Pharmaceutical Inc..
| Product ID | 49884-121_5f5d78fa-1989-4a3c-9434-8b0ecc240418 |
| NDC | 49884-121 |
| Proprietary Name | NDC 49884-121 |
| Marketing Start Date | 1983-09-27 |
| Marketing Category | / |
| Labeler Name | Par Pharmaceutical Inc. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA088391 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1983-09-27 |
| Marketing End Date | 2018-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA088391 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1983-09-27 |
| Marketing End Date | 2018-04-30 |
| Ingredient | Strength |
|---|---|
| HYDRALAZINE HYDROCHLORIDE | 100 mg/1 |