Package 0615-8188-39

Brand: ropinirole hydrochloride

Generic: ropinirole hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8188-39
Digits Only 0615818839
Product NDC 0615-8188
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8188-39)

Marketing

Marketing Status
Marketed Since 2018-03-05
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": "76b08d6e-992e-4f34-b803-7ed84025a75f", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845", "312846", "312847", "314208"], "spl_set_id": ["48a63d7e-c0af-4b09-863c-2af7beb2e80f"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8188-39)", "package_ndc": "0615-8188-39", "marketing_start_date": "20180305"}], "brand_name": "ROPINIROLE HYDROCHLORIDE", "product_id": "0615-8188_76b08d6e-992e-4f34-b803-7ed84025a75f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "0615-8188", "generic_name": "ROPINIROLE HYDROCHLORIDE", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE HYDROCHLORIDE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA090429", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20261231"}