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DIAZEPAM

NDC 11534-202, diazepam, tablet, from Sunrise Pharmaceutical, Inc..

Product NDC
11534-202
Status
Listed
Labeler
Sunrise Pharmaceutical, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070464
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11534-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIAZEPAM2 mg/1

Pharmacologic classes

Benzodiazepine [EPC]; Benzodiazepines [CS]

Package NDCNDC-11Package
11534-202-0111534020201100 TABLET in 1 BOTTLE (11534-202-01)
11534-202-03115340202031000 TABLET in 1 BOTTLE (11534-202-03)
11534-202-0411534020204500 TABLET in 1 BOTTLE (11534-202-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/34ac0b9d-d4ad-4aaa-8bee-902365f4e9a8

Use it

Look up 11534-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11534-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11534-202. 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.