Losartan Potassium - losartan potassium
Navigation: NDC > Supplier starting with: U > UDL LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 51079-751 |
| Proprietary Name: | Losartan Potassium |
| Suffix: | |
| Non-Proprietary Name: | losartan potassium |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 12-08-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA091590 |
| Labeler: | UDL LABORATORIES, INC. |
| Substance Name: | LOSARTAN POTASSIUM |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
| DEA Schedule: |