diclofenac sodium
- Product NDC
- 68788-8237
- 11-digit product format
- 687888237
- Labeler code
- 68788
- Product ID
- 68788-8237_632f553b-130a-4d45-8dcd-fe6fcf6a9ab8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA210893
- Marketing category
- ANDA
- Marketing start
- 2022-08-09
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 68788-8237 | DICLOFENAC SODIUM GEL [PREFERRED PHARMACEUTICALS INC.] | 4 | Legacy NDC | 20250321_632f553b-130a-4d45-8dcd-fe6fcf6a9ab8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8237-1 | 68788823701 | 1 TUBE in 1 CARTON (68788-8237-1) > 100 g in 1 TUBE | 1 tube | 2022-08-09 | 0000-00-00 | No | No | Current |