NDC 67296-2287
Tretinoin 0.25 mg per 1 g cream
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Northstar Rx LLC.'s NDC 16714-270.
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
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Tretinoin: every company that makes it
- Form
- cream, topical
- Strength
- 0.25 mg per 1 g
- Approval
- ANDA ANDA215713
- On the market since
- Jan 5, 2023
- Package NDCs
67296-2287-4- Official label
- DailyMed (National Library of Medicine), updated Jul 30, 2026
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