Diclofenac Sodium
- Product NDC
- 50090-7243
- 11-digit product format
- 500907243
- Labeler code
- 50090
- Product ID
- 50090-7243_1faca506-ccdc-4f83-8b18-5c80d320be4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium Topical Gel, 1%,
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210986
- Marketing category
- ANDA
- Marketing start
- 2020-01-30
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7243-0 | 50090724300 | 1 TUBE in 1 CARTON (50090-7243-0) / 100 g in 1 TUBE | 1 tube | 2024-09-11 | No | No | Historical |