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ropinirole
ropinirole - 68462-254-10 - (ropinirole)
Drug Information of ropinirole
| Product NDC: | 68462-254 |
| Proprietary Name: | ropinirole |
| Non Proprietary Name: | ropinirole |
| Active Ingredient(s): | .5 mg/1 & nbsp; ropinirole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ropinirole
| Product NDC: | 68462-254 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090135 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100225 |
Package Information of ropinirole
| Package NDC: | 68462-254-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-254-10) |
NDC Information of ropinirole
| NDC Code | 68462-254-10 |
| Proprietary Name | ropinirole |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-254-10) |
| Product NDC | 68462-254 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ropinirole |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100225 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | ROPINIROLE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
