| NDC Code | 49884-329-10 |
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| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-329-10) |
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| Product NDC | 49884-329 |
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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 |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20070126 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078065 |
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| Manufacturer | Par Pharmaceutical, Inc. |
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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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