| NDC Code | 46708-004-90 |
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| Package Description | 90 TABLET in 1 BOTTLE (46708-004-90) |
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| Product NDC | 46708-004 |
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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 | 20160322 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078894 |
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| Manufacturer | Alembic Pharmaceuticals Limited |
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| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
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| Strength | .25 |
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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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