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Ondansetron Hydrochloride

NDC 68788-8651, Ondansetron Hydrochloride, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8651
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-8651 \
  -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
68788-8651-16878886510110 TABLET, FILM COATED in 1 BOTTLE (68788-8651-1)
68788-8651-26878886510212 TABLET, FILM COATED in 1 BOTTLE (68788-8651-2)
68788-8651-36878886510330 TABLET, FILM COATED in 1 BOTTLE (68788-8651-3)
68788-8651-56878886510515 TABLET, FILM COATED in 1 BOTTLE (68788-8651-5)
68788-8651-66878886510660 TABLET, FILM COATED in 1 BOTTLE (68788-8651-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/36d64400-2d13-4a1a-a1ca-4741cd3d3f1a
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68788-8651

Use it

Look up 68788-8651 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8651 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8651. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.