NDC product
DUO Fusion
NDC 0597-0315 · Boehringer Ingelheim Pharmaceuticals, Inc.
Key facts
| Product NDC | 0597-0315 |
|---|---|
| Proprietary name | DUO Fusion |
| Labeler | Boehringer Ingelheim Pharmaceuticals, Inc. |
| Marketing category | ANDA |
| Application number | ANDA077355 |
| Marketing start | Mar 1, 2016 |
| Marketing end | Oct 29, 2021 |
| Listing certified through | Oct 29, 2021 |
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: