ondansetron
Generic: ondansetron
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
american health packaging
Dosage Form
SOLUTION
Routes
Active Ingredients
ondansetron hydrochloride 4 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
60687-252
Product ID
60687-252_43dfaa03-af7d-df4e-e063-6394a90a9f1e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091483
Marketing Start
2019-02-05
Marketing End
2027-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687252
Hyphenated Format
60687-252
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
ANDA091483 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/5mL
Packaging
- 3 TRAY in 1 CASE (60687-252-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-252-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-252-40)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43dfaa03-af7d-df4e-e063-6394a90a9f1e", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["312085"], "spl_set_id": ["92b96072-e8f2-4fd6-aaa0-b73fed214319"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (60687-252-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-252-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-252-40)", "package_ndc": "60687-252-86", "marketing_end_date": "20270131", "marketing_start_date": "20190205"}], "brand_name": "Ondansetron", "product_id": "60687-252_43dfaa03-af7d-df4e-e063-6394a90a9f1e", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "60687-252", "generic_name": "Ondansetron", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/5mL"}], "application_number": "ANDA091483", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20190205"}