NDC Code | 29300-401-01 |
Package Description | 100 TABLET in 1 BOTTLE (29300-401-01) |
Product NDC | 29300-401 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Atenolol And Chlorthalidone |
Non-Proprietary Name | Atenolol And Chlorthalidone |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20201125 |
Marketing Category Name | ANDA |
Application Number | ANDA213302 |
Manufacturer | Unichem Pharmaceuticals (USA), Inc. |
Substance Name | ATENOLOL; CHLORTHALIDONE |
Strength | 100; 25 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], beta-Adrenergic Blocker [EPC] |