Atenolol - Atenolol
Navigation: NDC > Supplier starting with: A > AUROLIFE PHARMA LLC| Field | Value |
|---|---|
| NDC Code: | 13107-169 |
| Proprietary Name: | Atenolol |
| Suffix: | |
| Non-Proprietary Name: | Atenolol |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 20-06-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA078512 |
| Labeler: | AUROLIFE PHARMA LLC |
| Substance Name: | ATENOLOL |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| DEA Schedule: |