ondansetron
Generic: ondansetron
Labeler: west-ward pharmaceuticals corpDrug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
west-ward pharmaceuticals corp
Dosage Form
INJECTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9890
Product ID
0143-9890_7dd1fe92-e406-4dde-a0e7-abfc496ccfc3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076781
Listing Expiration
2026-12-31
Marketing Start
2006-12-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439890
Hyphenated Format
0143-9890
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
ANDA076781 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 20 mL in 1 VIAL, MULTI-DOSE (0143-9890-01)
- 10 VIAL, MULTI-DOSE in 1 CARTON (0143-9890-10) / 20 mL in 1 VIAL, MULTI-DOSE (0143-9890-01)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "7dd1fe92-e406-4dde-a0e7-abfc496ccfc3", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["bb4bc810-db26-471b-9ce7-6e2fb3018af0"], "manufacturer_name": ["West-Ward Pharmaceuticals Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, MULTI-DOSE (0143-9890-01)", "package_ndc": "0143-9890-01", "marketing_start_date": "20061226"}, {"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0143-9890-10) / 20 mL in 1 VIAL, MULTI-DOSE (0143-9890-01)", "package_ndc": "0143-9890-10", "marketing_start_date": "20061226"}], "brand_name": "Ondansetron", "product_id": "0143-9890_7dd1fe92-e406-4dde-a0e7-abfc496ccfc3", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0143-9890", "generic_name": "Ondansetron", "labeler_name": "West-Ward Pharmaceuticals Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA076781", "marketing_category": "ANDA", "marketing_start_date": "20061226", "listing_expiration_date": "20261231"}