| NDC Code | 63739-535-10 |
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| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-535-10) > 10 TABLET in 1 BLISTER PACK |
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| Product NDC | 63739-535 |
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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 | 20120622 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091254 |
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| Manufacturer | McKesson Packaging Services a business unit of McKesson Corporation |
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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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