Package 70518-3482-0

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 70518-3482-0
Digits Only 7051834820
Product NDC 70518-3482
Product ID 70518-3482_3a9d5931-8ffb-d5e2-e063-6394a90a7edd
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3482-0)

Marketing

Marketing Status
Marketed Since 2022-08-17
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": "3a9d5931-8ffb-d5e2-e063-6394a90a7edd", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["314208"], "spl_set_id": ["864b38b0-1d4b-4da8-9645-c1760a2080ce"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3482-0)", "package_ndc": "70518-3482-0", "marketing_start_date": "20220817"}], "brand_name": "ropinirole", "product_id": "70518-3482_3a9d5931-8ffb-d5e2-e063-6394a90a7edd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "70518-3482", "generic_name": "ropinirole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA090135", "marketing_category": "ANDA", "marketing_start_date": "20220817", "listing_expiration_date": "20261231"}