Package 50090-1822-0

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 50090-1822-0
Digits Only 5009018220
Product NDC 50090-1822
Product ID 50090-1822_9928b6fc-9135-4260-b9e1-66a6d8c9a152
Description

100 TABLET, FILM COATED in 1 BOTTLE (50090-1822-0)

Marketing

Marketing Status
Marketed Since 2015-05-12
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

ropinirole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9928b6fc-9135-4260-b9e1-66a6d8c9a152", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845", "562704"], "spl_set_id": ["35d0074e-212b-4a1f-9cd7-974ca08d2c95"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-1822-0)", "package_ndc": "50090-1822-0", "marketing_start_date": "20150512"}], "brand_name": "ropinirole", "product_id": "50090-1822_9928b6fc-9135-4260-b9e1-66a6d8c9a152", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-1822", "generic_name": "ropinirole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA090135", "marketing_category": "ANDA", "marketing_start_date": "20100225", "listing_expiration_date": "20271231"}