| NDC Code | 23155-111-03 |
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| Package Description | 30 TABLET in 1 BOTTLE (23155-111-03) |
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| Product NDC | 23155-111 |
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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 | 20081013 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078955 |
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| Manufacturer | Heritage Pharmaceuticals Inc. |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 20 |
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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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