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Atenolol and Chlorthalidone
Atenolol and Chlorthalidone - 0591-5782-01 - (Atenolol and Chlorthalidone)
Drug Information of Atenolol and Chlorthalidone
| Product NDC: | 0591-5782 |
| Proprietary Name: | Atenolol and Chlorthalidone |
| Non Proprietary Name: | Atenolol and Chlorthalidone |
| Active Ingredient(s): | 50; 25 mg/1; mg/1 & nbsp; Atenolol and Chlorthalidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Atenolol and Chlorthalidone
| Product NDC: | 0591-5782 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073665 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19920801 |
Package Information of Atenolol and Chlorthalidone
| Package NDC: | 0591-5782-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0591-5782-01) |
NDC Information of Atenolol and Chlorthalidone
| NDC Code | 0591-5782-01 |
| Proprietary Name | Atenolol and Chlorthalidone |
| Package Description | 100 TABLET in 1 BOTTLE (0591-5782-01) |
| Product NDC | 0591-5782 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Atenolol and Chlorthalidone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19920801 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | ATENOLOL; CHLORTHALIDONE |
| Strength Number | 50; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
