| NDC Code | 68071-3031-2 |
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| Package Description | 20 TABLET in 1 BOTTLE (68071-3031-2) |
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| Product NDC | 68071-3031 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metoclopramide Hydrochloride |
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| Non-Proprietary Name | Metoclopramide Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20110822 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA071250 |
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| Manufacturer | NuCare Pharmaceuticals, Inc. |
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| Substance Name | METOCLOPRAMIDE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC] |
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