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Ondansetron

NDC 67296-2119, Ondansetron, tablet, film coated, from Redpharm Drug.

Product NDC
67296-2119
Status
Listed
Labeler
Redpharm Drug
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077535
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2119 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ONDANSETRON HYDROCHLORIDE4 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67296-2119-36729621190330 TABLET, FILM COATED in 1 BOTTLE (67296-2119-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/300b1916-a3d8-0220-e063-6394a90a6f55

Use it

Look up 67296-2119 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2119 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67296-2119. 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.