NDC product
POWDER · Megafine Pharma (P) Limited
NDC 22665-0015 · Megafine Pharma (P) Limited
Key facts
| Product NDC | 22665-0015 |
|---|---|
| Nonproprietary name | Memantine Hydrochloride |
| Substances | MEMANTINE HYDROCHLORIDE |
| Dosage form | POWDER |
| Labeler | Megafine Pharma (P) Limited |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Mar 24, 2011 |
| 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: