NDC 51991-649 is a in the category. It is labeled and distributed by Breckenridge Pharmaceutical, Inc..
| Product ID | 51991-649_8e5ce36b-8114-4925-9351-075b1d1ef2d4 |
| NDC | 51991-649 |
| Proprietary Name | NDC 51991-649 |
| Marketing Start Date | 2011-11-01 |
| Marketing Category | / |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA090511 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-11-01 |
| Marketing End Date | 2011-11-02 |
| Ingredient | Strength |
|---|---|
| LEVETIRACETAM | 750 mg/1 |