| NDC Code | 29300-210-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (29300-210-10) |
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| Product NDC | 29300-210 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pramipexole Dihydrochloride |
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| Non-Proprietary Name | Pramipexole Dihydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20190301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207011 |
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| Manufacturer | Unichem Pharmaceuticals (USA), Inc. |
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| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Dopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC] |
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