ondansetron
Generic: ondansetron
Labeler: gland pharma limitedDrug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
gland pharma limited
Dosage Form
INJECTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68083-113
Product ID
68083-113_89f78024-73fc-4243-a6d1-ae463b613b8c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079224
Listing Expiration
2026-12-31
Marketing Start
2009-09-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68083113
Hyphenated Format
68083-113
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
ANDA079224 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 5 VIAL in 1 CARTON (68083-113-01) / 2 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "89f78024-73fc-4243-a6d1-ae463b613b8c", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["3efa5604-96c3-42a0-8e99-b3de4a66aa92"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (68083-113-01) / 2 mL in 1 VIAL", "package_ndc": "68083-113-01", "marketing_start_date": "20090925"}], "brand_name": "Ondansetron", "product_id": "68083-113_89f78024-73fc-4243-a6d1-ae463b613b8c", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68083-113", "generic_name": "Ondansetron", "labeler_name": "Gland Pharma Limited", "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": "20090925", "listing_expiration_date": "20261231"}