Package 67296-2119-3

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 67296-2119-3
Digits Only 6729621193
Product NDC 67296-2119
Product ID 67296-2119_4698a594-cf21-0365-e063-6294a90a8784
Description

30 TABLET, FILM COATED in 1 BOTTLE (67296-2119-3)

Marketing

Marketing Status
Marketed Since 2007-06-25
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": "4698a594-cf21-0365-e063-6294a90a8784", "openfda": {"upc": ["0368462158111", "0368462106303"], "unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["300b1916-a3d8-0220-e063-6394a90a6f55"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-2119-3)", "package_ndc": "67296-2119-3", "marketing_start_date": "20070625"}], "brand_name": "Ondansetron", "product_id": "67296-2119_4698a594-cf21-0365-e063-6294a90a8784", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "67296-2119", "generic_name": "Ondansetron", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA077535", "marketing_category": "ANDA", "marketing_start_date": "20070625", "listing_expiration_date": "20261231"}