Package 50090-1330-0

Brand: ropinirole hydrochloride

Generic: ropinirole hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-1330-0
Digits Only 5009013300
Product NDC 50090-1330
Product ID 50090-1330_7cb28ad9-c0e7-42a6-9ce0-82ab6d0b6aa5
Description

100 TABLET, FILM COATED in 1 BOTTLE (50090-1330-0)

Marketing

Marketing Status
Marketed Since 2014-11-28
Brand ropinirole hydrochloride
Generic ropinirole hydrochloride
Sample Package No

Linked Drug Pages (1)

ropinirole hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7cb28ad9-c0e7-42a6-9ce0-82ab6d0b6aa5", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845"], "spl_set_id": ["9c4dacc6-cebc-4f42-85fc-41083512b290"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-1330-0)", "package_ndc": "50090-1330-0", "marketing_start_date": "20141128"}], "brand_name": "ropinirole hydrochloride", "product_id": "50090-1330_7cb28ad9-c0e7-42a6-9ce0-82ab6d0b6aa5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-1330", "generic_name": "ropinirole hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole hydrochloride", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA078110", "marketing_category": "ANDA", "marketing_start_date": "20110920", "listing_expiration_date": "20261231"}