NDC product
Eletriptan hydrobromide
NDC 68382-922 · Zydus Pharmaceuticals USA Inc.
Key facts
| Product NDC | 68382-922 |
|---|---|
| Proprietary name | Eletriptan hydrobromide |
| Nonproprietary name | Eletriptan hydrobromide |
| Substances | ELETRIPTAN HYDROBROMIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Zydus Pharmaceuticals USA Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA206409 |
| Pharmacologic classes | Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
| Marketing start | Jul 12, 2017 |
| Listing certified through | Dec 31, 2027 |
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: