NDC 0832-8302
Isotretinoin 20 mg capsule, liquid filled
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Douglas Manufacturing Limited | Lincoln Auckland, New Zealand | Makes it | Problems found, fixed voluntarilyMay 30, 2025 · 6 inspections |
Product details
- Generic drug
- Isotretinoin: every company that makes it
- Form
- capsule, liquid filled, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA076485
- On the market since
- May 1, 2012
- Package NDCs
0832-8302-300832-8302-89- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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