Diclofenac Sodium 1.5%
- Product NDC
- 71205-138
- 11-digit product format
- 712050138
- Labeler code
- 71205
- Product ID
- 71205-138_ba14e672-9223-4dfc-87dd-176e4988a9af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium Topical Solution
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA202769
- Marketing category
- ANDA
- Marketing start
- 2017-11-20
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16 mg/mL
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-138 | DICLOFENAC SODIUM 1.5% (DICLOFENAC SODIUM TOPICAL SOLUTION) SOLUTION [PROFICIENT RX LP] | 4 | Legacy NDC | 20210112_ac82c08f-a2e9-433c-92ea-bef724169f20.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-138-15 | 71205013815 | 150 mL in 1 BOTTLE (71205-138-15) | 150 ml | 2018-10-01 | 0000-00-00 | No | No | Current |