| NDC Code | 61990-0213-1 |
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| Package Description | 1 VIAL in 1 CARTON (61990-0213-1) > 10 mL in 1 VIAL (61990-0213-0) |
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| Product NDC | 61990-0213 |
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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 | 20200812 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211081 |
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| Manufacturer | Apollo Pharmaceuticals Inc. |
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| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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