| NDC Code | 68071-3065-3 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (68071-3065-3) |
|---|
| Product NDC | 68071-3065 |
|---|
| 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 | 19920801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA073665 |
|---|
| Manufacturer | NuCare Pharmaceuticals, Inc. |
|---|
| Substance Name | ATENOLOL; CHLORTHALIDONE |
|---|
| Strength | 50; 25 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide-like Diuretic [EPC], beta-Adrenergic Blocker [EPC] |
|---|