Package 76420-917-01

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-917-01
Digits Only 7642091701
Product NDC 76420-917
Description

1 BLISTER PACK in 1 CARTON (76420-917-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-01-28
Brand ondansetron hydrochloride
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cbe06c2-92c4-f72d-e063-6294a90aede8", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312084", "312086"], "spl_set_id": ["65b0b2e2-37fd-4d08-9674-954d62bb531a"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (76420-917-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "76420-917-01", "marketing_start_date": "20250128"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "76420-917_2cbe06c2-92c4-f72d-e063-6294a90aede8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "76420-917", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "24 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}