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Ondansetron

NDC 69339-172, Ondansetron, tablet, from Natco Pharma USA LLC.

Product NDC
69339-172
Status
Listed
Labeler
Natco Pharma USA LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077851
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69339-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ONDANSETRON HYDROCHLORIDE8 mg/1

Pharmacologic classes

Serotonin 3 Receptor Antagonists [MoA]; Serotonin-3 Receptor Antagonist [EPC]

Package NDCNDC-11Package
69339-172-0169339017201100 TABLET in 1 BOTTLE (69339-172-01)
69339-172-036933901720330 TABLET in 1 BOTTLE (69339-172-03)
69339-172-0569339017205500 TABLET in 1 BOTTLE (69339-172-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/64527de5-0b92-4340-9243-7a37e8ff96d9

  • NADAC price for package 69339017201

    GET /v1/drugs/nadac/69339017201

  • NADAC price for package 69339017203

    GET /v1/drugs/nadac/69339017203

Use it

Look up 69339-172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69339-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69339-172. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.