| NDC Code | 68462-332-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (68462-332-05) |
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| Product NDC | 68462-332 |
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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 | 20101008 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090781 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
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| Strength | .5 |
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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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