NDC product
POWDER · Cambrex Karlskoga AB
NDC 12651-120 · Cambrex Karlskoga AB
Key facts
| Product NDC | 12651-120 |
|---|---|
| Nonproprietary name | Berotralstat Dihydrochloride |
| Substances | BEROTRALSTAT DIHYDROCHLORIDE |
| Dosage form | POWDER |
| Labeler | Cambrex Karlskoga AB |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Jan 13, 2021 |
| Listing certified through | Dec 31, 2026 |
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: