NDC product
Naproxen sodium
NDC 55700-625 · Quality Care Products, LLC
Key facts
| Product NDC | 55700-625 |
|---|---|
| Proprietary name | Naproxen sodium |
| Nonproprietary name | Naproxen sodium |
| Substances | NAPROXEN SODIUM |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Quality Care Products, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA078486 |
| Pharmacologic classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| Marketing start | May 18, 2018 |
| Marketing end | Oct 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