Package 68071-3801-1

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 68071-3801-1
Digits Only 6807138011
Product NDC 68071-3801
Product ID 68071-3801_2eeb34c0-0917-f263-e063-6294a90ac1f2
Description

10 TABLET, FILM COATED in 1 BOTTLE (68071-3801-1)

Marketing

Marketing Status
Marketed Since 2025-02-24
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

Ondansetron ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2eeb34c0-0917-f263-e063-6294a90ac1f2", "openfda": {"upc": ["0368071380118"], "unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["2eeb3c61-4ce9-d8ed-e063-6294a90a00d3"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68071-3801-1)", "package_ndc": "68071-3801-1", "marketing_start_date": "20250224"}], "brand_name": "Ondansetron", "product_id": "68071-3801_2eeb34c0-0917-f263-e063-6294a90ac1f2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68071-3801", "generic_name": "Ondansetron", "labeler_name": "NuCare Pharmaceuticals, 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": "20210406", "listing_expiration_date": "20261231"}