| NDC Code | 62332-108-71 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-108-71) |
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| Product NDC | 62332-108 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ropinirole |
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| Non-Proprietary Name | Ropinirole |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20200620 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202786 |
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| Manufacturer | Alembic Pharmaceuticals Inc. |
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| Substance Name | ROPINIROLE HYDROCHLORIDE |
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| Strength | 4 |
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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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