Package 70518-4245-0

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 70518-4245-0
Digits Only 7051842450
Product NDC 70518-4245
Product ID 70518-4245_4007a856-78ce-2f62-e063-6394a90a1045
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4245-0)

Marketing

Marketing Status
Marketed Since 2024-12-20
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4007a856-78ce-2f62-e063-6394a90a1045", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["416be720-82e8-4a6d-8531-c1a29869daae"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4245-0)", "package_ndc": "70518-4245-0", "marketing_start_date": "20241220"}], "brand_name": "Ondansetron", "product_id": "70518-4245_4007a856-78ce-2f62-e063-6394a90a1045", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "70518-4245", "generic_name": "Ondansetron", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}