Package 72789-034-12

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-034-12
Digits Only 7278903412
Product NDC 72789-034
Product ID 72789-034_3c6d1f46-ae20-8bc0-e063-6394a90a4a08
Description

12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)

Marketing

Marketing Status
Marketed Since 2019-12-02
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": "3c6d1f46-ae20-8bc0-e063-6394a90a4a08", "openfda": {"upc": ["0372789034126"], "unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["426ba54f-199a-41d1-8c27-f827bea56854"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)", "package_ndc": "72789-034-12", "marketing_start_date": "20191202"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "72789-034_3c6d1f46-ae20-8bc0-e063-6394a90a4a08", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "72789-034", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}