NDC product
hydrocodone bitartrate and acetaminophen
NDC 10914-551 · Brighton Pharmaceuticals, Inc.
Key facts
| Product NDC | 10914-551 |
|---|---|
| Proprietary name | hydrocodone bitartrate and acetaminophen |
| Labeler | Brighton Pharmaceuticals, Inc. |
| Marketing category | ANDA |
| Application number | ANDA040556 |
| Marketing start | Jun 30, 2008 |
| Marketing end | May 12, 2013 |
| Listing certified through | May 12, 2013 |
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: