NDC product
Follistim AQ
NDC 0052-0316 · Merck Sharp & Dohme LLC
Key facts
| Product NDC | 0052-0316 |
|---|---|
| Proprietary name | Follistim AQ |
| Labeler | Merck Sharp & Dohme LLC |
| Marketing category | BLA |
| Application number | BLA021211 |
| Marketing start | Mar 24, 2004 |
| Marketing end | Apr 17, 2026 |
| Listing certified through | Apr 17, 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: