| NDC Code | 51655-302-26 |
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| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (51655-302-26) |
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| Product NDC | 51655-302 |
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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 | 20200519 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA070221 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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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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