United States · FDA National Drug Code directory
Azelaic Acid Gel
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0781-7172_d6c8343f-d169-4924-9fa2-4fbf097a32a7
- Product NDC
- 0781-7172
- Form
- GEL
- Composition / generic term
- azelaic acid
- Labeler
- Sandoz Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20181001
- Source listing expiry
- 20261231
Source-listed ingredients
- AZELAIC ACID — .15 g/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (0781-7172-50) / 50 g in 1 TUBE · 0781-7172-50
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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