Package 72162-2364-5

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2364-5
Digits Only 7216223645
Product NDC 72162-2364
Product ID 72162-2364_f671e80e-3772-4e5b-ac7f-ae463267ac2e
Description

500 TABLET, FILM COATED in 1 BOTTLE (72162-2364-5)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "f671e80e-3772-4e5b-ac7f-ae463267ac2e", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["e2c0e86c-e7fc-48f9-a894-02da8761001c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2364-5)", "package_ndc": "72162-2364-5", "marketing_start_date": "20240716"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "72162-2364_f671e80e-3772-4e5b-ac7f-ae463267ac2e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "72162-2364", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20271231"}