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Ondansetron

NDC 16714-159, Ondansetron, tablet, film coated, from NorthStar Rx LLC.

Product NDC
16714-159
Status
Listed
Labeler
NorthStar Rx 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/16714-159 \
  -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
16714-159-011671401590130 TABLET, FILM COATED in 1 BOTTLE (16714-159-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9d5e7650-95be-4b96-b29c-374f673eb7a1

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=16714-159

  • NADAC price for package 16714015901

    GET /v1/drugs/nadac/16714015901

Use it

Look up 16714-159 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-159 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-159. 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.