| NDC Code | 50111-469-03 |
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| Package Description | 1000 TABLET in 1 BOTTLE (50111-469-03) |
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| Product NDC | 50111-469 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propranolol Hydrochloride |
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| Non-Proprietary Name | Propranolol Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19900930 |
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| End Marketing Date | 20190430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA071974 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 40 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
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