NDC 50090-6819
Tretinoin 0.5 mg per 1 g cream
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Northstar Rx LLC.'s NDC 16714-249.
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
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Recalls
- Sep 25, 2026 · Class III · Sun Pharmaceutical Industries Inc
Failed Impurities/Degradation Specifications
Lots: Lot # AD96183, 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, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA211644
- On the market since
- Jan 25, 2019
- Package NDCs
50090-6819-0- Official label
- DailyMed (National Library of Medicine), updated Feb 2, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?