NDC Code | 35356-859-30 |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (35356-859-30) |
Product NDC | 35356-859 |
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 | 20130328 |
Marketing Category Name | ANDA |
Application Number | ANDA074203 |
Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | ATENOLOL; CHLORTHALIDONE |
Strength | 100; 25 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |