Package 16714-671-02

Brand: ondansetron

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-671-02
Digits Only 1671467102
Product NDC 16714-671
Product ID 16714-671_add9275d-a837-48f4-ab0b-01fc50e4545f
Description

1 BOTTLE, PLASTIC in 1 CARTON (16714-671-02) / 50 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2007-11-28
Brand ondansetron
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Ondansetron ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "add9275d-a837-48f4-ab0b-01fc50e4545f", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312085"], "spl_set_id": ["ac3dfb81-a4c7-4147-9374-c234153b7c51"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (16714-671-02)  / 50 mL in 1 BOTTLE, PLASTIC", "package_ndc": "16714-671-02", "marketing_start_date": "20071128"}], "brand_name": "Ondansetron", "product_id": "16714-671_add9275d-a837-48f4-ab0b-01fc50e4545f", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "16714-671", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/5mL"}], "application_number": "ANDA078776", "marketing_category": "ANDA", "marketing_start_date": "20071128", "listing_expiration_date": "20261231"}