| NDC Code | 0378-0731-01 |
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| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0731-01) |
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| Product NDC | 0378-0731 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propranolol Hydrochloride And Hydrochlorothiazide |
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| Non-Proprietary Name | Propranolol Hydrochloride And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19870304 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA070947 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
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| Strength | 40; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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