NDC product
Butalbital and Acetaminophen
NDC 13517-109 · e5 Pharma, LLC
Key facts
| Product NDC | 13517-109 |
|---|---|
| Proprietary name | Butalbital and Acetaminophen |
| Labeler | e5 Pharma, LLC |
| Marketing category | ANDA |
| Application number | ANDA203484 |
| Marketing start | Sep 13, 2016 |
| Marketing end | Jan 12, 2017 |
| Listing certified through | Jan 12, 2017 |
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: