ondansetron
Generic: ondansetron
Labeler: fosun pharma usa inc.Drug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
fosun pharma usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72266-123
Product ID
72266-123_1807c451-e39c-6291-e063-6294a90a4359
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079224
Listing Expiration
2026-12-31
Marketing Start
2019-04-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72266123
Hyphenated Format
72266-123
Supplemental Identifiers
RxCUI
UPC
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
ANDA079224 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 25 VIAL in 1 CARTON (72266-123-25) / 2 mL in 1 VIAL (72266-123-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "1807c451-e39c-6291-e063-6294a90a4359", "openfda": {"upc": ["0372266124012"], "unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["e3f22b7e-b6ad-4799-93c7-d30540cada85"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72266-123-25) / 2 mL in 1 VIAL (72266-123-01)", "package_ndc": "72266-123-25", "marketing_start_date": "20190402"}], "brand_name": "Ondansetron", "product_id": "72266-123_1807c451-e39c-6291-e063-6294a90a4359", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "72266-123", "generic_name": "Ondansetron", "labeler_name": "Fosun Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA079224", "marketing_category": "ANDA", "marketing_start_date": "20190402", "listing_expiration_date": "20261231"}