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Azelaic Acid

NDC 51672-1389, Azelaic Acid, gel, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1389
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210549
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1389 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZELAIC ACID.15 g/g

Pharmacologic classes

Decreased Protein Synthesis [PE]; Decreased Sebaceous Gland Activity [PE]

Package NDCNDC-11Package
51672-1389-3516721389031 TUBE in 1 CARTON (51672-1389-3) / 50 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4e9e95d-1ebd-44df-a91e-59819715659c

  • NADAC price for package 51672138903

    GET /v1/drugs/nadac/51672138903

Use it

Look up 51672-1389 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1389 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1389. 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.