ondansetron hydrochloride
Generic: ondansetron hydrochloride
Labeler: sportpharm llcDrug Facts
Product Profile
Brand Name
ondansetron hydrochloride
Generic Name
ondansetron hydrochloride
Labeler
sportpharm llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ondansetron hydrochloride 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
85766-006
Product ID
85766-006_49eea112-0a1a-5f02-e063-6294a90a1e2c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078539
Listing Expiration
2027-12-31
Marketing Start
2007-07-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85766006
Hyphenated Format
85766-006
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
- 4 mg/1
Packaging
- 1000 TABLET, FILM COATED in 1 BOTTLE (85766-006-00)
- 3 TABLET, FILM COATED in 1 BOTTLE (85766-006-03)
- 500 TABLET, FILM COATED in 1 BOTTLE (85766-006-05)
- 6 TABLET, FILM COATED in 1 BOTTLE (85766-006-06)
- 10 TABLET, FILM COATED in 1 BOTTLE (85766-006-10)
- 24 TABLET, FILM COATED in 1 BOTTLE (85766-006-24)
- 30 TABLET, FILM COATED in 1 BOTTLE (85766-006-30)
- 60 TABLET, FILM COATED in 1 BOTTLE (85766-006-60)
- 90 TABLET, FILM COATED in 1 BOTTLE (85766-006-90)
Packages (9)
85766-006-00
1000 TABLET, FILM COATED in 1 BOTTLE (85766-006-00)
85766-006-03
3 TABLET, FILM COATED in 1 BOTTLE (85766-006-03)
85766-006-05
500 TABLET, FILM COATED in 1 BOTTLE (85766-006-05)
85766-006-06
6 TABLET, FILM COATED in 1 BOTTLE (85766-006-06)
85766-006-10
10 TABLET, FILM COATED in 1 BOTTLE (85766-006-10)
85766-006-24
24 TABLET, FILM COATED in 1 BOTTLE (85766-006-24)
85766-006-30
30 TABLET, FILM COATED in 1 BOTTLE (85766-006-30)
85766-006-60
60 TABLET, FILM COATED in 1 BOTTLE (85766-006-60)
85766-006-90
90 TABLET, FILM COATED in 1 BOTTLE (85766-006-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49eea112-0a1a-5f02-e063-6294a90a1e2c", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["b1324076-f83e-4816-9e02-6b2a689010bc"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (85766-006-00)", "package_ndc": "85766-006-00", "marketing_start_date": "20250619"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (85766-006-03)", "package_ndc": "85766-006-03", "marketing_start_date": "20250619"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (85766-006-05)", "package_ndc": "85766-006-05", "marketing_start_date": "20250619"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (85766-006-06)", "package_ndc": "85766-006-06", "marketing_start_date": "20250619"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (85766-006-10)", "package_ndc": "85766-006-10", "marketing_start_date": "20250619"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (85766-006-24)", "package_ndc": "85766-006-24", "marketing_start_date": "20251001"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85766-006-30)", "package_ndc": "85766-006-30", "marketing_start_date": "20250619"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85766-006-60)", "package_ndc": "85766-006-60", "marketing_start_date": "20250619"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85766-006-90)", "package_ndc": "85766-006-90", "marketing_start_date": "20250619"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "85766-006_49eea112-0a1a-5f02-e063-6294a90a1e2c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "85766-006", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20271231"}