Package 70518-3511-1

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3511-1
Digits Only 7051835111
Product NDC 70518-3511
Product ID 70518-3511_4588cfcf-6654-7206-e063-6394a90a4d6c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-1)

Marketing

Marketing Status
Marketed Since 2025-07-02
Brand ondansetron hydrochloride
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Ondansetron Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4588cfcf-6654-7206-e063-6394a90a4d6c", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["5cc67d95-6629-4451-9e34-2f7a60482be5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-0)", "package_ndc": "70518-3511-0", "marketing_start_date": "20220906"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-1)", "package_ndc": "70518-3511-1", "marketing_start_date": "20250702"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "70518-3511_4588cfcf-6654-7206-e063-6394a90a4d6c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "70518-3511", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20220906", "listing_expiration_date": "20261231"}