Diclofenac sodium
- Product NDC
- 71335-0371
- 11-digit product format
- 713350371
- Labeler code
- 71335
- Product ID
- 71335-0371_c4347399-f89a-41f7-84b0-6bc8e7db3edc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208077
- Marketing category
- ANDA
- Marketing start
- 2016-03-21
- 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
- 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 |
|---|
| 71335-0371-1 | 71335037101 | 1 g in 1 BOTTLE (71335-0371-1) | 1 g | 2016-03-21 | 0000-00-00 | No | No | Current |