| NDC Code | 0703-4502-93 |
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| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0703-4502-93) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-91) |
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| Product NDC | 0703-4502 |
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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 |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20240904 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA073135 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC] |
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