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Clorazepate Dipotassium

NDC 51672-4044, Clorazepate Dipotassium, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4044
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075731
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4044 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CLORAZEPATE DIPOTASSIUM15 mg/1

Pharmacologic classes

Benzodiazepine [EPC]; Benzodiazepines [CS]

Package NDCNDC-11Package
51672-4044-151672404401100 TABLET in 1 BOTTLE (51672-4044-1)
51672-4044-251672404402500 TABLET in 1 BOTTLE (51672-4044-2)
51672-4044-3516724044031000 TABLET in 1 BOTTLE (51672-4044-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/499a6989-8912-44b7-b1eb-ee8f85ae378f

  • NADAC price for package 51672404401

    GET /v1/drugs/nadac/51672404401

Use it

Look up 51672-4044 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4044 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4044. 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.