NDC product
SUPPRELIN LA
NDC 67979-002 · Endo USA, Inc.
Key facts
| Product NDC | 67979-002 |
|---|---|
| Proprietary name | SUPPRELIN |
| Nonproprietary name | histrelin acetate |
| Substances | HISTRELIN ACETATE |
| Dosage form | IMPLANT |
| Route | SUBCUTANEOUS |
| Labeler | Endo USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA022058 |
| Pharmacologic classes | Gonadotropin Releasing Hormone Receptor Agonist [EPC], Gonadotropin Releasing Hormone Receptor Agonists [MoA] |
| Marketing start | May 31, 2007 |
| 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: