Diclofenac Sodium
- Product NDC
- 50090-7839
- 11-digit product format
- 500907839
- Labeler code
- 50090
- Product ID
- 50090-7839_a3bd8225-950c-4beb-a9cf-65264ba310d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075185
- Marketing category
- ANDA
- Marketing start
- 2025-03-28
- Substance
- DICLOFENAC SODIUM
- Active strength
- 75 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| QTG126297Q | DICLOFENAC SODIUM | 15307-79-6 | DICLOFENAC SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7839-0 | 50090783900 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7839-0) | 2025-12-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Diclofenac Sodium | A-S Medication Solutions | 2025-12-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |