Package 43547-274-50
Brand: ropinirole hydrochloride
Generic: ropinirole hydrochloridePackage Facts
Identity
Package NDC
43547-274-50
Digits Only
4354727450
Product NDC
43547-274
Description
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-274-50)
Marketing
Marketing Status
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": "0e04048a-c22c-4c6b-9c00-91906541a95a", "openfda": {"upc": ["0343547274108", "0343547271107", "0343547269104", "0343547270100", "0343547272104", "0343547273101", "0343547268107"], "unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["7734ef0b-584f-42dd-a8b5-adbdf4e4df93"], "manufacturer_name": ["SOLCO HEALTHCARE US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-274-10)", "package_ndc": "43547-274-10", "marketing_start_date": "20110920"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-274-50)", "package_ndc": "43547-274-50", "marketing_start_date": "20110920"}], "brand_name": "ropinirole hydrochloride", "product_id": "43547-274_0e04048a-c22c-4c6b-9c00-91906541a95a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "43547-274", "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": "5 mg/1"}], "application_number": "ANDA078110", "marketing_category": "ANDA", "marketing_start_date": "20110920", "listing_expiration_date": "20261231"}