Package 76420-917-01
Brand: ondansetron hydrochloride
Generic: ondansetron hydrochloridePackage 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
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"}