Package 70518-4318-0

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 70518-4318-0
Digits Only 7051843180
Product NDC 70518-4318
Product ID 70518-4318_402e5750-a88f-8dfe-e063-6394a90afe1d
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4318-0)

Marketing

Marketing Status
Marketed Since 2025-03-25
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "402e5750-a88f-8dfe-e063-6394a90afe1d", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312846"], "spl_set_id": ["cdc63b7a-062a-4519-a63e-e48a356f641c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4318-0)", "package_ndc": "70518-4318-0", "marketing_start_date": "20250325"}], "brand_name": "Ropinirole", "product_id": "70518-4318_402e5750-a88f-8dfe-e063-6394a90afe1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "70518-4318", "generic_name": "Ropinirole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA079229", "marketing_category": "ANDA", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}