| NDC Code | 51662-1338-1 |
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| Package Description | 1 mL in 1 VIAL (51662-1338-1) |
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| Product NDC | 51662-1338 |
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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 | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20181222 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077760 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
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