NDC product
Azelaic Acid Gel
NDC 0781-7172 · Sandoz Inc.
Key facts
| Product NDC | 0781-7172 |
|---|---|
| Proprietary name | Azelaic Acid Gel |
| Nonproprietary name | azelaic acid |
| Substances | AZELAIC ACID |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Sandoz Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA021470 |
| Pharmacologic classes | Decreased Protein Synthesis [PE], Decreased Sebaceous Gland Activity [PE] |
| Marketing start | Oct 1, 2018 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: