Package 50090-4803-0

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 50090-4803-0
Digits Only 5009048030
Product NDC 50090-4803
Description

100 TABLET, FILM COATED in 1 BOTTLE (50090-4803-0)

Marketing

Marketing Status
Marketed Since 2019-12-20
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "964359dc-018a-469d-a2e6-cf5191a4b2ec", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845"], "spl_set_id": ["4f4729f8-c910-4a09-a4b4-b4243e7f0105"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4803-0)", "package_ndc": "50090-4803-0", "marketing_start_date": "20191220"}], "brand_name": "ropinirole", "product_id": "50090-4803_964359dc-018a-469d-a2e6-cf5191a4b2ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-4803", "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": "ANDA204022", "marketing_category": "ANDA", "marketing_start_date": "20181017", "listing_expiration_date": "20261231"}