ondansetron
Generic: ondansetron
Labeler: henry schein, inc.Drug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
henry schein, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0404-9930
Product ID
0404-9930_87fe0041-54b9-4cef-83b1-41f7d0d9232d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203711
Listing Expiration
2026-12-31
Marketing Start
2022-01-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04049930
Hyphenated Format
0404-9930
Supplemental Identifiers
RxCUI
UNII
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
ANDA203711 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 1 VIAL, SINGLE-USE in 1 BAG (0404-9930-02) / 2 mL in 1 VIAL, SINGLE-USE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "87fe0041-54b9-4cef-83b1-41f7d0d9232d", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["1a44601b-c31c-4779-a688-28cc4cc75e8b"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 BAG (0404-9930-02) / 2 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0404-9930-02", "marketing_start_date": "20220113"}], "brand_name": "ONDANSETRON", "product_id": "0404-9930_87fe0041-54b9-4cef-83b1-41f7d0d9232d", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0404-9930", "generic_name": "ONDANSETRON", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA203711", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}