ondansetron
Generic: ondansetron
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
a-s medication solutions
Dosage Form
INJECTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4935
Product ID
50090-4935_14702c7a-4a84-4cec-a0dc-0b70c13939d7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203711
Listing Expiration
2026-12-31
Marketing Start
2016-05-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904935
Hyphenated Format
50090-4935
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
- 25 VIAL, SINGLE-USE in 1 CARTON (50090-4935-0) / 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": "14702c7a-4a84-4cec-a0dc-0b70c13939d7", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["b60074e5-8e77-4dc0-9244-4205e4adbaef"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 CARTON (50090-4935-0) / 2 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50090-4935-0", "marketing_start_date": "20200227"}], "brand_name": "ONDANSETRON", "product_id": "50090-4935_14702c7a-4a84-4cec-a0dc-0b70c13939d7", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "50090-4935", "generic_name": "ONDANSETRON", "labeler_name": "A-S Medication Solutions", "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": "20160526", "listing_expiration_date": "20261231"}