Diclofenac Sodium
- Product NDC
- 71205-752
- 11-digit product format
- 712050752
- Labeler code
- 71205
- Product ID
- 71205-752_b41335b6-859f-4568-84d2-0d0408415a4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206493
- Marketing category
- ANDA
- Marketing start
- 2016-05-19
- Substance
- DICLOFENAC SODIUM
- Active strength
- 30 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 |
|---|
| 71205-752-00 | 71205075200 | 1 TUBE in 1 CARTON (71205-752-00) / 100 g in 1 TUBE | 1 tube | 2023-02-02 | No | No | Historical |