NDC 51672-1363 – Diclofenac sodium
Diclofenac Sodium 30 mg/g · Gel · Topical
Product NDC51672-1363
Product details
- Brand name
- Diclofenac sodium
- Generic name
- Diclofenac sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Gel
- Route
- Topical
- Marketing category
- ANDA · ANDA206298
- Marketed since
- April 28, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Diclofenac Sodium 30 mg/g
Uses, dosage, side effects and warnings for Diclofenac Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1363-3 | 1 TUBE in 1 CARTON (51672-1363-3) / 50 g in 1 TUBE | Apr 28, 2016 |
| 51672-1363-7 | 1 TUBE in 1 CARTON (51672-1363-7) / 100 g in 1 TUBE | Apr 28, 2016 |
Recalls mentioning this NDC
- D-0342-2026 Feb 11, 2026 · Class II
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
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