| NDC Code | 60687-581-21 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-581-21) / 1 TABLET in 1 BLISTER PACK (60687-581-11) |
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| Product NDC | 60687-581 |
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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 | 20200813 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090865 |
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| Manufacturer | American Health Packaging |
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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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