Package 42708-179-05

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-179-05
Digits Only 4270817905
Product NDC 42708-179
Product ID 42708-179_4653a20b-ee05-d476-e063-6394a90ab9d4
Description

5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-179-05)

Marketing

Marketing Status
Marketed Since 2023-05-19
Brand ondansetron hydrochloride
Generic ondansetron hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Ondansetron Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4653a20b-ee05-d476-e063-6394a90ab9d4", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["fbe71308-2927-2467-e053-6394a90aa419"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-179-05)", "package_ndc": "42708-179-05", "marketing_start_date": "20230519"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "42708-179_4653a20b-ee05-d476-e063-6394a90ab9d4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "42708-179", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}