ondansetron hydrochloride
Generic: ondansetron hydrochloride
Labeler: sportpharm, inc. dba sportpharmDrug Facts
Product Profile
Brand Name
ondansetron hydrochloride
Generic Name
ondansetron hydrochloride
Labeler
sportpharm, inc. dba sportpharm
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ondansetron hydrochloride 8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
85766-053
Product ID
85766-053_4018fab5-2d3a-48e6-e063-6394a90a43b9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078539
Listing Expiration
2026-12-31
Marketing Start
2007-07-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85766053
Hyphenated Format
85766-053
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 hydrochloride (source: ndc)
Generic Name
ondansetron hydrochloride (source: ndc)
Application Number
ANDA078539 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8 mg/1
Packaging
- 5 TABLET, FILM COATED in 1 BOTTLE (85766-053-05)
- 10 TABLET, FILM COATED in 1 BOTTLE (85766-053-10)
- 14 TABLET, FILM COATED in 1 BOTTLE (85766-053-14)
- 20 TABLET, FILM COATED in 1 BOTTLE (85766-053-20)
- 24 TABLET, FILM COATED in 1 BOTTLE (85766-053-24)
- 30 TABLET, FILM COATED in 1 BOTTLE (85766-053-30)
- 60 TABLET, FILM COATED in 1 BOTTLE (85766-053-60)
- 90 TABLET, FILM COATED in 1 BOTTLE (85766-053-90)
Packages (8)
85766-053-05
5 TABLET, FILM COATED in 1 BOTTLE (85766-053-05)
85766-053-10
10 TABLET, FILM COATED in 1 BOTTLE (85766-053-10)
85766-053-14
14 TABLET, FILM COATED in 1 BOTTLE (85766-053-14)
85766-053-20
20 TABLET, FILM COATED in 1 BOTTLE (85766-053-20)
85766-053-24
24 TABLET, FILM COATED in 1 BOTTLE (85766-053-24)
85766-053-30
30 TABLET, FILM COATED in 1 BOTTLE (85766-053-30)
85766-053-60
60 TABLET, FILM COATED in 1 BOTTLE (85766-053-60)
85766-053-90
90 TABLET, FILM COATED in 1 BOTTLE (85766-053-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4018fab5-2d3a-48e6-e063-6394a90a43b9", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["c0be25a0-e13d-4242-93dc-0b86e82aadd7"], "manufacturer_name": ["Sportpharm, Inc. dba Sportpharm"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (85766-053-05)", "package_ndc": "85766-053-05", "marketing_start_date": "20251001"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (85766-053-10)", "package_ndc": "85766-053-10", "marketing_start_date": "20251001"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (85766-053-14)", "package_ndc": "85766-053-14", "marketing_start_date": "20251001"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (85766-053-20)", "package_ndc": "85766-053-20", "marketing_start_date": "20251001"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (85766-053-24)", "package_ndc": "85766-053-24", "marketing_start_date": "20251001"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85766-053-30)", "package_ndc": "85766-053-30", "marketing_start_date": "20251001"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85766-053-60)", "package_ndc": "85766-053-60", "marketing_start_date": "20251001"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85766-053-90)", "package_ndc": "85766-053-90", "marketing_start_date": "20251001"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "85766-053_4018fab5-2d3a-48e6-e063-6394a90a43b9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "85766-053", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Sportpharm, Inc. dba Sportpharm", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}