Diclofenac sodium
- Product NDC
- 50268-237
- 11-digit product format
- 502680237
- Labeler code
- 50268
- Product ID
- 50268-237_bc7b6137-2577-3a38-e053-2a95a90adfce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- AvPAK
- Application
- ANDA208077
- Marketing category
- ANDA
- Marketing start
- 2021-03-01
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 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
- 2022-12-31
- 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 |
|---|
| 50268-237-20 | 50268023720 | 20 TUBE in 1 BOX (50268-237-20) > 2 g in 1 TUBE (50268-237-11) | 20 tube | 2021-03-01 | 0000-00-00 | No | No | Current |