| NDC Code | 70069-812-10 |
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| Package Description | 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-812-10) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-812-01) |
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| Product NDC | 70069-812 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phenylephrine Hydrochloride |
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| Non-Proprietary Name | Phenylephrine Hydrochloride |
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| Dosage Form | INJECTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20230717 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213318 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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