NDC product
Acyclovir
NDC 81288-039 · EMC PHARMA, LLC
Key facts
| Product NDC | 81288-039 |
|---|---|
| Proprietary name | Acyclovir |
| Labeler | EMC PHARMA, LLC |
| Marketing category | ANDA |
| Application number | ANDA212173 |
| Marketing start | Jul 29, 2022 |
| Marketing end | May 30, 2025 |
| Listing certified through | May 30, 2025 |
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: