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Lomustine

NDC 52536-340, lomustine, capsule, gelatin coated, from Wilshire Pharmaceuticals, Inc..

Product NDC
52536-340
Status
Listed
Labeler
Wilshire Pharmaceuticals, Inc.
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA017588
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52536-340 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOMUSTINE10 mg/1

Pharmacologic classes

Alkylating Activity [MoA]; Alkylating Drug [EPC]

Package NDCNDC-11Package
52536-340-05525360340051 BOTTLE in 1 CARTON (52536-340-05) / 5 CAPSULE, GELATIN COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3c3637fc-4499-4331-a3c4-6969fc86704e

Use it

Look up 52536-340 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52536-340 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52536-340. 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.