Package 0641-6286-01

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 0641-6286-01
Digits Only 0641628601
Product NDC 0641-6286
Product ID 0641-6286_65dafe3e-7450-46dd-932f-6fff7e4e58b6
Description

20 mL in 1 VIAL, MULTI-DOSE (0641-6286-01)

Marketing

Marketing Status
Marketed Since 2006-12-26
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": "65dafe3e-7450-46dd-932f-6fff7e4e58b6", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["97713356-f42b-4a67-95f6-561afa68c0c2"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, MULTI-DOSE (0641-6286-01)", "package_ndc": "0641-6286-01", "marketing_start_date": "20061226"}], "brand_name": "Ondansetron", "product_id": "0641-6286_65dafe3e-7450-46dd-932f-6fff7e4e58b6", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0641-6286", "generic_name": "Ondansetron", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA077365", "marketing_category": "ANDA", "marketing_start_date": "20061226", "listing_expiration_date": "20261231"}