NDC 68071-2674
Tretinoin 0.5 mg per 1 g cream
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1394.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Sep 25, 2026 · Class III · Sun Pharmaceutical Industries Inc
Failed Impurities/Degradation Specifications
Lots: Lot # AD96184, Exp Date: 12/31/2026. - Sep 25, 2026 · Class III · Sun Pharmaceutical Industries Inc
Failed Impurities/Degradation Specifications
Lots: Lot # AD96196, Exp Date: 12/31/2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Tretinoin: every company that makes it
- Form
- cream
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA211644
- On the market since
- Jan 25, 2019
- Package NDCs
68071-2674-4- Official label
- DailyMed (National Library of Medicine), updated Apr 25, 2022
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