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Capecitabine

NDC 62756-238, Capecitabine, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-238
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204668
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-238 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CAPECITABINE150 mg/1

Pharmacologic classes

Nucleic Acid Synthesis Inhibitors [MoA]; Nucleoside Metabolic Inhibitor [EPC]

Package NDCNDC-11Package
62756-238-18627560238181000 TABLET, FILM COATED in 1 BOTTLE (62756-238-18)
62756-238-866275602388660 TABLET, FILM COATED in 1 BOTTLE (62756-238-86)
62756-238-8862756023888100 TABLET, FILM COATED in 1 BOTTLE (62756-238-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e3b1a2b5-f1ce-45ea-afd8-68aac53665fa

Use it

Look up 62756-238 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-238 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-238. 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.