NDC product
Methylphenidate Hydrochloride
NDC 55466-101 · Neolpharma, Inc.
Key facts
| Product NDC | 55466-101 |
|---|---|
| Proprietary name | Methylphenidate Hydrochloride |
| Labeler | Neolpharma, Inc. |
| Marketing category | ANDA |
| Application number | ANDA208737 |
| Marketing start | Mar 29, 2024 |
| Marketing end | Mar 29, 2024 |
| Listing certified through | Mar 29, 2024 |
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: