Package 42708-059-05

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-059-05
Digits Only 4270805905
Product NDC 42708-059
Product ID 42708-059_4652e75e-e926-67a7-e063-6294a90a850c
Description

5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05)

Marketing

Marketing Status
Marketed Since 2018-04-19
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": "4652e75e-e926-67a7-e063-6294a90a850c", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["dafe875e-391f-47a2-97b7-89840a760e44"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05)", "package_ndc": "42708-059-05", "marketing_start_date": "20180419"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "42708-059_4652e75e-e926-67a7-e063-6294a90a850c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "42708-059", "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"}