NDC product
Pramipexole Dihydrochloride
NDC 0555-0615 · Barr Laboratories Inc.
Key facts
| Product NDC | 0555-0615 |
|---|---|
| Proprietary name | Pramipexole Dihydrochloride |
| Labeler | Barr Laboratories Inc. |
| Marketing category | ANDA |
| Application number | ANDA077724 |
| Marketing start | Jan 4, 2010 |
| Marketing end | Nov 22, 2013 |
| Listing certified through | Nov 22, 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: