Package 16729-232-01

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 16729-232-01
Digits Only 1672923201
Product NDC 16729-232
Product ID 16729-232_23980eef-2eb5-2b74-e063-6394a90a68ac
Description

100 TABLET, FILM COATED in 1 BOTTLE (16729-232-01)

Marketing

Marketing Status
Marketed Since 2018-10-17
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": "23980eef-2eb5-2b74-e063-6394a90a68ac", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["4a2a5b63-5b14-6975-e054-00144ff8d46c"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16729-232-01)", "package_ndc": "16729-232-01", "marketing_start_date": "20181017"}], "brand_name": "ropinirole", "product_id": "16729-232_23980eef-2eb5-2b74-e063-6394a90a68ac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "16729-232", "generic_name": "ropinirole", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA204022", "marketing_category": "ANDA", "marketing_start_date": "20181017", "listing_expiration_date": "20261231"}