Package 71610-119-88

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-119-88
Digits Only 7161011988
Product NDC 71610-119
Product ID 71610-119_864f5aaf-0819-42bb-8bc6-7878a5378986
Description

900 TABLET, FILM COATED in 1 BOTTLE (71610-119-88)

Marketing

Marketing Status
Marketed Since 2018-08-15
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": "864f5aaf-0819-42bb-8bc6-7878a5378986", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["08db5ce7-4dcf-4581-a0bf-f405cc22b48d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "900 TABLET, FILM COATED in 1 BOTTLE (71610-119-88)", "package_ndc": "71610-119-88", "marketing_start_date": "20180815"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "71610-119_864f5aaf-0819-42bb-8bc6-7878a5378986", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71610-119", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}