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ONDANSETRON

NDC 51662-1678, ONDANSETRON, tablet, film coated, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1678
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076183
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1678 \
  -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
51662-1678-15166216780130 TABLET, FILM COATED in 1 BOTTLE (51662-1678-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4dcd1e4c-6a9c-7ac6-e063-6394a90a39bf

Use it

Look up 51662-1678 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1678 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1678. 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.