| NDC Code | 52584-051-90 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-051-90) > 20 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 52584-051 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dobutamine Hydrochloride |
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| Non-Proprietary Name | Dobutamine Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20100301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074277 |
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| Manufacturer | General Injectables & Vaccines, Inc |
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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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