ondansetron

Generic: ondansetron

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron
Generic Name ondansetron
Labeler american health packaging
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

ondansetron hydrochloride 4 mg/5mL

Manufacturer
American Health Packaging

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
serotonin 3 receptor antagonists [moa] serotonin-3 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687252
Hyphenated Format 60687-252

Supplemental Identifiers

RxCUI
312085
UNII
NMH84OZK2B

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/5mL
source: ndc
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)
source: ndc

Packages (1)

Ingredients (1)

ondansetron hydrochloride (4 mg/5mL)

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"}