Package 50090-7445-0

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 50090-7445-0
Digits Only 5009074450
Product NDC 50090-7445
Product ID 50090-7445_d8869312-010a-4fa5-a6d4-6df0b21dc881
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)

Marketing

Marketing Status
Marketed Since 2024-11-06
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": "d8869312-010a-4fa5-a6d4-6df0b21dc881", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["562704"], "spl_set_id": ["339a961e-4eb0-4406-913e-ccc9e9bde084"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7445-0)", "package_ndc": "50090-7445-0", "marketing_start_date": "20241106"}], "brand_name": "Ropinirole", "product_id": "50090-7445_d8869312-010a-4fa5-a6d4-6df0b21dc881", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-7445", "generic_name": "Ropinirole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA079229", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}