Package 23155-549-31

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 23155-549-31
Digits Only 2315554931
Product NDC 23155-549
Product ID 23155-549_a9ae0d2e-667a-4c29-8697-32b044725d35
Description

1 VIAL in 1 CARTON (23155-549-31) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2012-06-15
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

ONDANSETRON ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a9ae0d2e-667a-4c29-8697-32b044725d35", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["b746d4db-43e6-4219-9e6b-f53e59581305"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (23155-549-31)  / 20 mL in 1 VIAL", "package_ndc": "23155-549-31", "marketing_start_date": "20120615"}], "brand_name": "ONDANSETRON", "product_id": "23155-549_a9ae0d2e-667a-4c29-8697-32b044725d35", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "23155-549", "generic_name": "ONDANSETRON", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA090648", "marketing_category": "ANDA", "marketing_start_date": "20120615", "listing_expiration_date": "20271231"}