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Ropinirole
Ropinirole - 55111-659-05 - (Ropinirole)
Drug Information of Ropinirole
| Product NDC: | 55111-659 |
| Proprietary Name: | Ropinirole |
| Non Proprietary Name: | Ropinirole |
| Active Ingredient(s): | 2 mg/1 & nbsp; Ropinirole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ropinirole
| Product NDC: | 55111-659 |
| Labeler Name: | Dr. Reddys Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201576 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120606 |
Package Information of Ropinirole
| Package NDC: | 55111-659-05 |
| Package Description: | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-659-05) |
NDC Information of Ropinirole
| NDC Code | 55111-659-05 |
| Proprietary Name | Ropinirole |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-659-05) |
| Product NDC | 55111-659 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ropinirole |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120606 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddys Laboratories Limited |
| Substance Name | ROPINIROLE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
