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Cladribine

NDC 0781-8201, Cladribine, tablet, from Sandoz Inc..

Product NDC
0781-8201
Status
Listed
Labeler
Sandoz Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215547
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8201 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CLADRIBINE10 mg/1

Pharmacologic classes

Purine Antimetabolite [EPC]

Package NDCNDC-11Package
0781-8201-37007818201379 TABLET in 1 CARTON (0781-8201-37)
0781-8201-51007818201515 TABLET in 1 CARTON (0781-8201-51)
0781-8201-68007818201686 TABLET in 1 CARTON (0781-8201-68)
0781-8201-71007818201717 TABLET in 1 CARTON (0781-8201-71)
0781-8201-800078182018010 TABLET in 1 CARTON (0781-8201-80)
0781-8201-85007818201858 TABLET in 1 CARTON (0781-8201-85)
0781-8201-94007818201944 TABLET in 1 CARTON (0781-8201-94)

Linked data

RxNorm, label and prices

Use it

Look up 0781-8201 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8201 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-8201. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.