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ROPINIROLE HYDROCHLORIDE
ROPINIROLE HYDROCHLORIDE - 64720-205-10 - (ROPINIROLE HYDROCHLORIDE)
Drug Information of ROPINIROLE HYDROCHLORIDE
| Product NDC: | 64720-205 |
| Proprietary Name: | ROPINIROLE HYDROCHLORIDE |
| Non Proprietary Name: | ROPINIROLE HYDROCHLORIDE |
| Active Ingredient(s): | 3 mg/1 & nbsp; ROPINIROLE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ROPINIROLE HYDROCHLORIDE
| Product NDC: | 64720-205 |
| Labeler Name: | Corepharma LLC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078230 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080521 |
Package Information of ROPINIROLE HYDROCHLORIDE
| Package NDC: | 64720-205-10 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (64720-205-10) |
NDC Information of ROPINIROLE HYDROCHLORIDE
| NDC Code | 64720-205-10 |
| Proprietary Name | ROPINIROLE HYDROCHLORIDE |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (64720-205-10) |
| Product NDC | 64720-205 |
| 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 | Corepharma LLC. |
| Substance Name | ROPINIROLE HYDROCHLORIDE |
| Strength Number | 3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
