| NDC Code: |
0904-6200 |
| Proprietary Name: |
Atenolol and Chlorthalidone |
| Suffix: |
|
| Non-Proprietary Name: |
Atenolol and Chlorthalidone |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
29-04-1993 |
| Category Name: |
ANDA |
| Application Number: |
ANDA073582 |
| Labeler: |
MAJOR PHARMACEUTICAL |
| Substance Name: |
ATENOLOL; CHLORTHALIDONE |
| Active Numerator Strength: |
50; 25 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
| DEA Schedule: |
|
