Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | India | Makes it and tests it | Problems found, fixed voluntarilyMay 12, 2023 · 1 inspection |
| Reed-Lane, Inc. | Wayne, NJ, United States | Packages it | No problems foundOct 17, 2025 · 7 inspections |
Recalls
- May 22, 2017 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specifications: out of specification results observed for low dissolution.
Lots: Lot #: KB50414, KB50456, Exp 05/17; KB50457, KB50458, KB50459, KB50460, Exp 06/17; KB50580, KB50581, KB50582, KB50583, KB50599, KB50600, Exp 07/17; KB50646, KB50647, KB50721, KB50722, KB50723, KB50724, Exp 09/17; KB50833, KB50834, KB50835, KB50836, KB50837, Exp 10/17; KB50902, KB50903, KB50904, Exp…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Isotretinoin: every company that makes it
- Form
- capsule, gelatin coated, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA202099
- On the market since
- Mar 9, 2015
- Package NDCs
55111-113-7855111-113-7955111-113-81- Official label
- DailyMed (National Library of Medicine), updated Sep 20, 2026
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