| NDC Code | 53808-0772-1 |
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| Package Description | 30 TABLET in 1 BLISTER PACK (53808-0772-1) |
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| Product NDC | 53808-0772 |
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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 | 20090701 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA070177 |
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| Manufacturer | State of Florida DOH Central Pharmacy |
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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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