Package 43547-600-50

Brand: ropinirole hydrochloride

Generic: ropinirole hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43547-600-50
Digits Only 4354760050
Product NDC 43547-600
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-600-50)

Marketing

Marketing Status
Marketed Since 2011-09-20
Brand ropinirole hydrochloride
Generic ropinirole hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bb48dd84-da25-4221-bdc7-2039e4300ed3", "openfda": {"upc": ["0343547601102", "0343547598105", "0343547596101", "0343547597108", "0343547599102", "0343547595104", "0343547600105"], "unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["5823b3a2-3256-4d94-97b4-ec6b940312f4"], "manufacturer_name": ["SOLCO HEALTHCARE US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-600-10)", "package_ndc": "43547-600-10", "marketing_start_date": "20110920"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-600-50)", "package_ndc": "43547-600-50", "marketing_start_date": "20110920"}], "brand_name": "ropinirole hydrochloride", "product_id": "43547-600_bb48dd84-da25-4221-bdc7-2039e4300ed3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "43547-600", "generic_name": "ropinirole hydrochloride", "labeler_name": "SOLCO HEALTHCARE US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole hydrochloride", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078110", "marketing_category": "ANDA", "marketing_start_date": "20110920", "listing_expiration_date": "20261231"}