Package 68083-114-01

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 68083-114-01
Digits Only 6808311401
Product NDC 68083-114
Description

1 VIAL in 1 CARTON (68083-114-01) / 20 mL in 1 VIAL

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2f33d54b-c852-4bca-ab80-a2852c1be9b8", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504"], "spl_set_id": ["35716914-ac73-43c0-9aa0-09c99211d941"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68083-114-01)  / 20 mL in 1 VIAL", "package_ndc": "68083-114-01", "marketing_start_date": "20120615"}], "brand_name": "Ondansetron", "product_id": "68083-114_2f33d54b-c852-4bca-ab80-a2852c1be9b8", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68083-114", "generic_name": "Ondansetron", "labeler_name": "Gland Pharma Limited", "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": "20261231"}