NDC 60687-583
Carbamazepine 200 mg tablet, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-681.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it and tests it | Problems found, fixed voluntarilyOct 23, 2022 · 6 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Sep 15, 2025 · Class II · Amerisource Health Services LLC
Failed Dissolution Specifications.
Lots: Lot #: 1024078, Exp. Date 08/31/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Carbamazepine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA211623
- On the market since
- Jan 5, 2022
- Package NDCs
60687-583-1160687-583-21- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?