Diclofenac Sodium
- Product NDC
- 68071-4382
- 11-digit product format
- 680714382
- Labeler code
- 68071
- Product ID
- 68071-4382_bb7bdc98-4f5d-83d5-e053-2a95a90a7feb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- NDA022122
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-07-01
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4382-1 | 68071438201 | 100 g in 1 BOX (68071-4382-1) | 100 g | 2018-04-09 | 0000-00-00 | No | No | Current |