Diclofenac Sodium
- Product NDC
- 68788-7518
- 11-digit product format
- 687887518
- Labeler code
- 68788
- Product ID
- 68788-7518_2fd175ea-df47-42ba-af17-ee2884352607
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA206493
- Marketing category
- ANDA
- Marketing start
- 2016-05-19
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 30 mg/g
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7518-1 | 68788751801 | 1 TUBE in 1 CARTON (68788-7518-1) > 100 g in 1 TUBE | 1 tube | 2019-10-25 | 0000-00-00 | No | No | Current |