NDC product
Doxepin HCL
NDC 72189-388 · Direct_Rx
Key facts
| Product NDC | 72189-388 |
|---|---|
| Proprietary name | Doxepin HCL |
| Labeler | Direct_Rx |
| Marketing category | ANDA |
| Application number | ANDA215483 |
| Marketing start | Oct 19, 2022 |
| Marketing end | Dec 18, 2024 |
| Listing certified through | Dec 18, 2024 |
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: