Package 55111-662-90
Brand: ropinirole
Generic: ropinirolePackage Facts
Identity
Package NDC
55111-662-90
Digits Only
5511166290
Product NDC
55111-662
Description
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-662-90)
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": "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 (55111-662-05)", "package_ndc": "55111-662-05", "marketing_start_date": "20120606"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-662-30)", "package_ndc": "55111-662-30", "marketing_start_date": "20120606"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-662-90)", "package_ndc": "55111-662-90", "marketing_start_date": "20120606"}], "brand_name": "Ropinirole", "product_id": "55111-662_78d63517-2d1a-fc70-4ffb-3ebbfa065218", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "55111-662", "generic_name": "Ropinirole", "labeler_name": "Dr. Reddys Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA201576", "marketing_category": "ANDA", "marketing_start_date": "20120606", "listing_expiration_date": "20261231"}