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Ondansetron Hydrochloride

NDC 82804-257, Ondansetron Hydrochloride, tablet, film coated, from Proficient Rx LP.

Product NDC
82804-257
Status
Listed
Labeler
Proficient Rx LP
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/82804-257 \
  -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
82804-257-108280402571010 TABLET, FILM COATED in 1 BOTTLE (82804-257-10)
82804-257-158280402571515 TABLET, FILM COATED in 1 BOTTLE (82804-257-15)
82804-257-308280402573030 TABLET, FILM COATED in 1 BOTTLE (82804-257-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0a14eb9a-0385-40e9-a7ec-71435450ac91

Use it

Look up 82804-257 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-257 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-257. 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.