Package 72162-2200-1

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 72162-2200-1
Digits Only 7216222001
Product NDC 72162-2200
Product ID 72162-2200_8b049ebc-b842-4f07-ac6f-eb4bf350240a
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2200-1)

Marketing

Marketing Status
Marketed Since 2023-12-15
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": "8b049ebc-b842-4f07-ac6f-eb4bf350240a", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312846"], "spl_set_id": ["e9ba4108-7095-4771-840e-bf1e08b5f4da"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2200-1)", "package_ndc": "72162-2200-1", "marketing_start_date": "20231215"}], "brand_name": "Ropinirole", "product_id": "72162-2200_8b049ebc-b842-4f07-ac6f-eb4bf350240a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "72162-2200", "generic_name": "Ropinirole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA079229", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}