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Ondansetron Hydrochloride

NDC 67046-1242, Ondansetron Hydrochloride, tablet, film coated, from Coupler LLC.

Product NDC
67046-1242
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078539
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1242 \
  -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
67046-1242-36704612420330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1242-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/546191d2-d092-6342-e063-6294a90a0cd3

Use it

Look up 67046-1242 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1242 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1242. 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.