Package 72189-364-30

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 72189-364-30
Digits Only 7218936430
Product NDC 72189-364
Product ID 72189-364_2c4c8dd5-f07a-0339-e063-6394a90afedb
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)

Marketing

Marketing Status
Marketed Since 2022-06-21
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": "2c4c8dd5-f07a-0339-e063-6394a90afedb", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845"], "spl_set_id": ["e1fb0b51-4f8a-965d-e053-2a95a90ad936"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)", "package_ndc": "72189-364-30", "marketing_start_date": "20220621"}], "brand_name": "Ropinirole", "product_id": "72189-364_2c4c8dd5-f07a-0339-e063-6394a90afedb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "72189-364", "generic_name": "Ropinirole", "labeler_name": "Direct_Rx", "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": "20220621", "listing_expiration_date": "20261231"}