NDC product
Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate
NDC 0722-6670 · Nexgen Pharma, Inc.
Key facts
| Product NDC | 0722-6670 |
|---|---|
| Proprietary name | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
| Labeler | Nexgen Pharma, Inc. |
| Marketing category | ANDA |
| Application number | ANDA076560 |
| Marketing start | Jun 10, 2004 |
| Listing certified through | Dec 31, 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: