Package 72189-222-30
Brand: ropinirole
Generic: ropinirolePackage Facts
Identity
Package NDC
72189-222-30
Digits Only
7218922230
Product NDC
72189-222
Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
Marketing
Marketing Status
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": "2c28281e-fe37-b7e4-e063-6294a90ad4f7", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["314208"], "spl_set_id": ["c2c38b4c-b139-45f2-e053-2995a90a262c"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)", "package_ndc": "72189-222-30", "marketing_start_date": "20210520"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)", "package_ndc": "72189-222-60", "marketing_start_date": "20210520"}], "brand_name": "ROPINIROLE", "product_id": "72189-222_2c28281e-fe37-b7e4-e063-6294a90ad4f7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "72189-222", "generic_name": "ROPINIROLE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA204022", "marketing_category": "ANDA", "marketing_start_date": "20210520", "listing_expiration_date": "20261231"}