| NDC Code | 55111-659-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-659-30) |
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| Product NDC | 55111-659 |
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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 | 20120606 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201576 |
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| Manufacturer | Dr. Reddys Laboratories Limited |
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| Substance Name | ROPINIROLE HYDROCHLORIDE |
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| Strength | 2 |
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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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