NDC product
HYLENEX Recombinant
NDC 18657-117 · Antares Pharma, Inc.
Key facts
| Product NDC | 18657-117 |
|---|---|
| Proprietary name | HYLENEX Recombinant |
| Nonproprietary name | Hyaluronidase |
| Substances | HYALURONIDASE (HUMAN RECOMBINANT) |
| Dosage form | INJECTION, SOLUTION |
| Route | SUBCUTANEOUS |
| Labeler | Antares Pharma, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Application number | BLA021859 |
| Pharmacologic classes | Endoglycosidase [EPC], Glycoside Hydrolases [CS] |
| Marketing start | Dec 2, 2005 |
| 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: