NDC product
TABLET, FILM COATED · Merck Sharp & Dohme LLC.
NDC 0006-0001 · Merck Sharp & Dohme LLC.
Key facts
| Product NDC | 0006-0001 |
|---|---|
| Nonproprietary name | suvorexant |
| Substances | SUVOREXANT |
| Dosage form | TABLET, FILM COATED |
| Labeler | Merck Sharp & Dohme LLC. |
| Product type | DRUG FOR FURTHER PROCESSING |
| Marketing category | DRUG FOR FURTHER PROCESSING |
| DEA schedule | CIV |
| Marketing start | Aug 15, 2014 |
| 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: