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ondansetron hydrochloride

NDC 62756-131, ondansetron hydrochloride, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-131
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077050
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-131 \
  -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
62756-131-016275601310130 TABLET, FILM COATED in 1 BOTTLE (62756-131-01)
62756-131-026275601310210 BLISTER PACK in 1 DOSE PACK (62756-131-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/92c758a3-e749-4a15-be4b-ee30b364b2b0

Use it

Look up 62756-131 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-131. 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.