Product NDC: | 64679-154 |
Proprietary Name: | Ropinirole Hydrochloride |
Non Proprietary Name: | Ropinirole Hydrochloride |
Active Ingredient(s): | .25 mg/1 & nbsp; Ropinirole Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64679-154 |
Labeler Name: | Wockhardt USA LLC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079050 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080529 |
Package NDC: | 64679-154-04 |
Package Description: | 10 BLISTER PACK in 1 CARTON (64679-154-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 64679-154-04 |
Proprietary Name | Ropinirole Hydrochloride |
Package Description | 10 BLISTER PACK in 1 CARTON (64679-154-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 64679-154 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ropinirole Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20080529 |
Marketing Category Name | ANDA |
Labeler Name | Wockhardt USA LLC. |
Substance Name | ROPINIROLE HYDROCHLORIDE |
Strength Number | .25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |