Package 60687-588-01

Brand: ropinirole hydrochloride

Generic: ropinirole hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-588-01
Digits Only 6068758801
Product NDC 60687-588
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-588-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-588-11)

Marketing

Marketing Status
Marketed Since 2021-06-09
Brand ropinirole hydrochloride
Generic ropinirole hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b3300f7-07e8-7648-e063-6394a90a3d62", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845", "314208"], "spl_set_id": ["6849b3c0-e36b-4bea-82f2-b33ae3d44c95"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-588-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-588-11)", "package_ndc": "60687-588-01", "marketing_start_date": "20210609"}], "brand_name": "ropinirole hydrochloride", "product_id": "60687-588_2b3300f7-07e8-7648-e063-6394a90a3d62", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "60687-588", "generic_name": "ropinirole hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole hydrochloride", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA078110", "marketing_category": "ANDA", "marketing_start_date": "20210609", "listing_expiration_date": "20261231"}