| NDC Code | 30256-017-01 |
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| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (30256-017-01) |
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| Product NDC | 30256-017 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Requip |
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| Proprietary Name Suffix | Xl |
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| Non-Proprietary Name | Ropinirole Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20080630 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA022008 |
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| Manufacturer | Glaxo Wellcome SA |
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| Substance Name | ROPINIROLE HYDROCHLORIDE |
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| Strength | 8 |
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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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