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Azelaic Acid Gel

NDC 0781-7172, azelaic acid, gel, from Sandoz Inc..

Product NDC
0781-7172
Status
Listed
Labeler
Sandoz Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021470
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-7172 \
  -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
0781-7172-50007817172501 TUBE in 1 CARTON (0781-7172-50) / 50 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/66178511-5c1a-4ecd-bc98-2ceb54e710ac

  • NADAC price for package 00781717250

    GET /v1/drugs/nadac/00781717250

Use it

Look up 0781-7172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-7172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-7172. 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.