NDC product
STRENSIQ
NDC 25682-013 · Alexion Pharmaceuticals, Inc.
Key facts
| Product NDC | 25682-013 |
|---|---|
| Proprietary name | STRENSIQ |
| Nonproprietary name | ASFOTASE ALFA |
| Substances | ASFOTASE ALFA |
| Dosage form | SOLUTION |
| Route | SUBCUTANEOUS |
| Labeler | Alexion Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Application number | BLA125513 |
| Pharmacologic classes | Alkaline Phosphatase [CS], Tissue-nonspecific Alkaline Phosphatase [EPC] |
| Marketing start | Oct 23, 2015 |
| 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: