NDC Code | 53489-532-10 |
Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-532-10) |
Product NDC | 53489-532 |
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 | 19930429 |
Marketing Category Name | ANDA |
Application Number | ANDA073582 |
Manufacturer | Mutual Pharmaceutical Company, Inc. |
Substance Name | ATENOLOL; CHLORTHALIDONE |
Strength | 100; 25 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Thiazide-like Diuretic [EPC],Increased Diuresis [PE] |