Package 0228-3640-03
Brand: ropinirole
Generic: ropinirolePackage Facts
Identity
Package NDC
0228-3640-03
Digits Only
0228364003
Product NDC
0228-3640
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3640-03)
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": "3499549d-d3ad-4636-8234-2539c0fbfac1", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["799054", "799055", "799056", "824959", "848582"], "spl_set_id": ["300946bf-2f83-471d-868d-9820b65c52bb"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-3640-03)", "package_ndc": "0228-3640-03", "marketing_start_date": "20120823"}], "brand_name": "Ropinirole", "product_id": "0228-3640_3499549d-d3ad-4636-8234-2539c0fbfac1", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "0228-3640", "generic_name": "Ropinirole", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA090869", "marketing_category": "ANDA", "marketing_start_date": "20120823", "listing_expiration_date": "20261231"}