| NDC Code | 17856-8728-1 |
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| Package Description | 50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP |
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| Product NDC | 17856-8728 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 19870515 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA070979 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
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