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ropinirole hydrochloride
ropinirole hydrochloride - 43547-272-10 - (ropinirole hydrochloride)
Drug Information of ropinirole hydrochloride
| Product NDC: | 43547-272 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ropinirole hydrochloride
| Product NDC: | 43547-272 |
| Labeler Name: | Solco Healthcare US LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078110 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110920 |
Package Information of ropinirole hydrochloride
| Package NDC: | 43547-272-10 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-272-10) |
NDC Information of ropinirole hydrochloride
| NDC Code | 43547-272-10 |
| Proprietary Name | ropinirole hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-272-10) |
| Product NDC | 43547-272 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ropinirole hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110920 |
| Marketing Category Name | ANDA |
| Labeler Name | Solco Healthcare US LLC |
| Substance Name | ROPINIROLE HYDROCHLORIDE |
| Strength Number | 3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
