Package 0904-6373-61

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 0904-6373-61
Digits Only 0904637361
Product NDC 0904-6373
Product ID 0904-6373_91c699dd-e272-4845-b550-1abdd74cf9b6
Description

100 BLISTER PACK in 1 CARTON (0904-6373-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-10-01
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

ROPINIROLE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "91c699dd-e272-4845-b550-1abdd74cf9b6", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845", "314208"], "spl_set_id": ["e7ef58c0-73ba-4af2-b82b-a33954ec44df"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6373-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6373-61", "marketing_start_date": "20141001"}], "brand_name": "ROPINIROLE", "product_id": "0904-6373_91c699dd-e272-4845-b550-1abdd74cf9b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "0904-6373", "generic_name": "ROPINIROLE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA090429", "marketing_category": "ANDA", "marketing_start_date": "20141001", "listing_expiration_date": "20261231"}