| NDC Code | 76045-101-20 |
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| Package Description | 24 BLISTER PACK in 1 CARTON (76045-101-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-101-00) / 2 mL in 1 SYRINGE, GLASS |
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| Product NDC | 76045-101 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metoclopramide |
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| Non-Proprietary Name | Metoclopramide Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20130503 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091392 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/2mL |
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| Pharmacy Classes | Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC] |
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