NDC product
memantine hydrochloride
NDC 0591-3900 · Actavis Pharma, Inc.
Key facts
| Product NDC | 0591-3900 |
|---|---|
| Proprietary name | memantine hydrochloride |
| Nonproprietary name | memantine hydrochloride |
| Dosage form | KIT |
| Route | ORAL |
| Labeler | Actavis Pharma, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA021487 |
| Marketing start | Apr 1, 2015 |
| Marketing end | Aug 31, 2028 |
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