NDC 68788-4147
Enalapril Maleate 20 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-688.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it and tests it | No problems foundMar 7, 2025 · 2 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Recalls
- Apr 23, 2026 · Class II · JB Chemicals and Pharmaceuticals Ltd
Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities Test
Lots: Lot #: GEH25023, Expires: 6/30/2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Enalaprilat: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA218531
- On the market since
- Jul 10, 2026
- Package NDCs
68788-4147-068788-4147-368788-4147-668788-4147-9- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2026
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