| NDC Code | 71205-761-90 |
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| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-761-90) |
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| Product NDC | 71205-761 |
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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 | 20070810 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078494 |
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| Manufacturer | Proficient Rx LP |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 120 |
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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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