| NDC Code | 54868-6159-0 |
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| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-6159-0) |
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| Product NDC | 54868-6159 |
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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 | 20100823 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077724 |
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| Manufacturer | Physicians Total Care, Inc. |
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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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