ondansetron
Generic: ondansetron
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-4759
Product ID
0409-4759_f4d4b538-f4fd-49d7-ac02-b72d48c52e59
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077473
Listing Expiration
2026-12-31
Marketing Start
2006-11-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04094759
Hyphenated Format
0409-4759
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ondansetron (source: ndc)
Generic Name
ondansetron (source: ndc)
Application Number
ANDA077473 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (0409-4759-01) / 20 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "f4d4b538-f4fd-49d7-ac02-b72d48c52e59", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["6a11f61b-2318-4382-2b91-4366e4bb53fa"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0409-4759-01) / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0409-4759-01", "marketing_start_date": "20061107"}], "brand_name": "Ondansetron", "product_id": "0409-4759_f4d4b538-f4fd-49d7-ac02-b72d48c52e59", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0409-4759", "generic_name": "ONDANSETRON", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA077473", "marketing_category": "ANDA", "marketing_start_date": "20061107", "listing_expiration_date": "20261231"}