Diclofenac Sodium
- Product NDC
- 71335-1226
- 11-digit product format
- 713351226
- Labeler code
- 71335
- Product ID
- 71335-1226_80fd69b0-ae14-4722-986b-57a6ed00482f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209903
- Marketing category
- ANDA
- Marketing start
- 2018-08-16
- 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
- 2020-12-31
- 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 |
|---|
| 71335-1226-1 | 71335122601 | 1 g in 1 BOTTLE (71335-1226-1) | 1 g | 2019-05-16 | 0000-00-00 | No | No | Current |