Package 55111-661-90

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 55111-661-90
Digits Only 5511166190
Product NDC 55111-661
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-90)

Marketing

Marketing Status
Marketed Since 2012-06-06
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": "78d63517-2d1a-fc70-4ffb-3ebbfa065218", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["799054", "799055", "799056", "824959", "848582"], "spl_set_id": ["ec0612a1-ccb1-bb51-8881-04faf491e093"], "manufacturer_name": ["Dr. Reddys Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-05)", "package_ndc": "55111-661-05", "marketing_start_date": "20120606"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-30)", "package_ndc": "55111-661-30", "marketing_start_date": "20120606"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-661-90)", "package_ndc": "55111-661-90", "marketing_start_date": "20120606"}], "brand_name": "Ropinirole", "product_id": "55111-661_78d63517-2d1a-fc70-4ffb-3ebbfa065218", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "55111-661", "generic_name": "Ropinirole", "labeler_name": "Dr. Reddys Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA201576", "marketing_category": "ANDA", "marketing_start_date": "20120606", "listing_expiration_date": "20261231"}