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Ondansetron Hydrochloride

NDC 43063-792, Ondansetron Hydrochloride, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-792
Status
Listed
Labeler
PD-Rx 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/43063-792 \
  -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
43063-792-06430630792066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0b675b09-fe40-435c-b91a-c61cdf767fbf

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=43063-792

Use it

Look up 43063-792 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-792 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-792. 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.