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Capecitabine

NDC 68001-644, Capecitabine, tablet, film coated, from BluePoint Laboratories.

Product NDC
68001-644
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210203
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-644 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CAPECITABINE500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68001-644-0768001064407120 TABLET, FILM COATED in 1 BOTTLE (68001-644-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/88c5af84-900a-4372-b056-bfea70c129cf

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68001-644

  • NADAC price for package 68001064407

    GET /v1/drugs/nadac/68001064407

Use it

Look up 68001-644 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-644 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-644. 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.