NDC product
Diclofenac Sodium Gel
NDC 72189-473 · Direct_Rx
Key facts
| Product NDC | 72189-473 |
|---|---|
| Proprietary name | Diclofenac Sodium Gel |
| Nonproprietary name | Diclofenac Sodium Gel |
| Substances | DICLOFENAC SODIUM |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Direct_Rx |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA212351 |
| Pharmacologic classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC] |
| Marketing start | May 19, 2023 |
| Listing certified through | Dec 31, 2027 |
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: