Product NDC: | 21695-798 |
Proprietary Name: | ROPINIROLE HYDROCHLORIDE |
Non Proprietary Name: | ROPINIROLE HYDROCHLORIDE |
Active Ingredient(s): | 5 mg/1 & nbsp; ROPINIROLE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-798 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078230 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080521 |
Package NDC: | 21695-798-60 |
Package Description: | 60 TABLET, COATED in 1 BOTTLE, PLASTIC (21695-798-60) |
NDC Code | 21695-798-60 |
Proprietary Name | ROPINIROLE HYDROCHLORIDE |
Package Description | 60 TABLET, COATED in 1 BOTTLE, PLASTIC (21695-798-60) |
Product NDC | 21695-798 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ROPINIROLE HYDROCHLORIDE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20080521 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | ROPINIROLE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |