Package 67046-1489-3

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 67046-1489-3
Digits Only 6704614893
Product NDC 67046-1489
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1489-3)

Marketing

Marketing Status
Marketed Since 2025-01-29
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": "2cdaf99a-56b8-4d61-e063-6294a90a3bc3", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312847"], "spl_set_id": ["2cdae415-479b-c14c-e063-6394a90adb6c"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1489-3)", "package_ndc": "67046-1489-3", "marketing_start_date": "20250129"}], "brand_name": "ROPINIROLE", "product_id": "67046-1489_2cdaf99a-56b8-4d61-e063-6294a90a3bc3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "67046-1489", "generic_name": "ROPINIROLE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA090429", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}