| NDC Code | 51991-820-05 |
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| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05) |
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| Product NDC | 51991-820 |
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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 | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20130311 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078703 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 160 |
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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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