| NDC Code | 14335-172-01 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (14335-172-01) > 40 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 14335-172 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dobutamine |
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| Non-Proprietary Name | Dobutamine |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210601 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA216131 |
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| Manufacturer | Hainan Poly Pharm. Co., Ltd. |
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| Substance Name | DOBUTAMINE HYDROCHLORIDE |
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| Strength | 12.5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Adrenergic beta-Agonists [MoA], beta-Adrenergic Agonist [EPC] |
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