Sun Pharma Canada Inc.
Brampton, Canada · makes it
No problems found Last FDA inspection Mar 27, 2026. 7 inspections on record.
NDC 50436-0356
Diclofenac sodium 30 mg per 1 g gel
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1363.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it
Recalls
- Jan 27, 2026 · Class II · Ongoing
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
Lots: Lot # AD92721, Exp Date: 3/31/2027.
Product details
- Generic drug
- Diclofenac: see every company that makes it
- Form
- gel
- Strength
- 30 mg per 1 g
- Approval
- ANDA ANDA206298
- On the market since
- Apr 28, 2016
- Package NDCs
50436-0356-1- Official label
- DailyMed (National Library of Medicine), updated Feb 10, 2023
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