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Ropinirole Hydrochloride
Ropinirole Hydrochloride - 0591-3613-05 - (Ropinirole Hydrochloride)
Drug Information of Ropinirole Hydrochloride
| Product NDC: | 0591-3613 |
| Proprietary Name: | Ropinirole Hydrochloride |
| Non Proprietary Name: | Ropinirole Hydrochloride |
| Active Ingredient(s): | 4 mg/1 & nbsp; Ropinirole Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ropinirole Hydrochloride
| Product NDC: | 0591-3613 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200431 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120606 |
Package Information of Ropinirole Hydrochloride
| Package NDC: | 0591-3613-05 |
| Package Description: | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3613-05) |
NDC Information of Ropinirole Hydrochloride
| NDC Code | 0591-3613-05 |
| Proprietary Name | Ropinirole Hydrochloride |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3613-05) |
| Product NDC | 0591-3613 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ropinirole Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120606 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | ROPINIROLE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
