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Ondansetron Hydrochloride

NDC 55700-631, Ondansetron Hydrochloride, tablet, film coated, from Quality Care Products LLC.

Product NDC
55700-631
Status
Listed
Labeler
Quality Care Products 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/55700-631 \
  -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
55700-631-105570006311010 TABLET, FILM COATED in 1 BOTTLE (55700-631-10)
55700-631-205570006312020 TABLET, FILM COATED in 1 BOTTLE (55700-631-20)
55700-631-305570006313030 TABLET, FILM COATED in 1 BOTTLE (55700-631-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/89091629-d15e-4e95-aed8-8bc983c78302

Use it

Look up 55700-631 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55700-631 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55700-631. 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.