Diclofenac sodium
- Product NDC
- 16714-976
- 11-digit product format
- 167140976
- Labeler code
- 16714
- Product ID
- 16714-976_af6641b9-53c9-44b1-a5e2-68644c62f5c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA209903
- Marketing category
- ANDA
- Marketing start
- 2019-12-10
- 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 |
|---|
| 16714-976-01 | 16714097601 | 1 TUBE in 1 CARTON (16714-976-01) > 100 g in 1 TUBE | 1 tube | 2019-12-10 | 0000-00-00 | No | No | Current |