Package 72189-416-30

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 72189-416-30
Digits Only 7218941630
Product NDC 72189-416
Product ID 72189-416_2c4cfec2-fee0-e007-e063-6294a90a3cf9
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-416-30)

Marketing

Marketing Status
Marketed Since 2023-02-01
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": "2c4cfec2-fee0-e007-e063-6294a90a3cf9", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845"], "spl_set_id": ["f3a9982a-015a-1134-e053-2a95a90ad2d4"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-416-30)", "package_ndc": "72189-416-30", "marketing_start_date": "20230201"}], "brand_name": "Ropinirole", "product_id": "72189-416_2c4cfec2-fee0-e007-e063-6294a90a3cf9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "72189-416", "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": "ANDA090135", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}