NDC product
Acetazolamide
NDC 51672-4022 · Sun Pharmaceutical Industries, Inc.
Key facts
| Product NDC | 51672-4022 |
|---|---|
| Proprietary name | Acetazolamide |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Marketing category | ANDA |
| Application number | ANDA040195 |
| Marketing start | May 28, 1997 |
| Marketing end | Nov 30, 2025 |
| Listing certified through | Nov 30, 2025 |
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: