| NDC Code | 70934-922-30 |
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| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (70934-922-30) |
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| Product NDC | 70934-922 |
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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 | 20211112 |
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| End Marketing Date | 20231231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA070322 |
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| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 10 |
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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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