NDC 68788-4164
Enalapril Maleate 5 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-686.
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
- 5 mg
- Approval
- ANDA ANDA218531
- On the market since
- Jul 23, 2026
- Package NDCs
68788-4164-168788-4164-368788-4164-668788-4164-9- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?