Diclofenac Sodium
- Product NDC
- 71205-450
- 11-digit product format
- 712050450
- Labeler code
- 71205
- Product ID
- 71205-450_7bc185e2-e749-4a24-8550-c2f6d39222d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA202769
- Marketing category
- ANDA
- Marketing start
- 2018-07-31
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16.05 mg/mL
- 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 |
|---|
| 71205-450-15 | 71205045015 | 1 BOTTLE in 1 CARTON (71205-450-15) / 150 mL in 1 BOTTLE | 1 bottle | 2020-04-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Diclofenac Sodium | Proficient Rx LP | 2020-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |