ondansetron
Generic: ondansetron hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
ondansetron hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-777
Product ID
25021-777_dbbafc2b-987e-421b-bcfc-d4706859420e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079224
Listing Expiration
2026-12-31
Marketing Start
2012-08-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021777
Hyphenated Format
25021-777
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 hydrochloride (source: ndc)
Application Number
ANDA079224 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 25 VIAL in 1 CARTON (25021-777-02) / 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": "dbbafc2b-987e-421b-bcfc-d4706859420e", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["1740467"], "spl_set_id": ["ba0f8f13-1f7d-44e0-9c0f-0b43a9e8e3a7"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-777-02) / 2 mL in 1 VIAL", "package_ndc": "25021-777-02", "marketing_start_date": "20120830"}], "brand_name": "ondansetron", "product_id": "25021-777_dbbafc2b-987e-421b-bcfc-d4706859420e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "25021-777", "generic_name": "ondansetron hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "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": "20120830", "listing_expiration_date": "20261231"}