NDC 68151-1364
Amlodipine Besylate and Benazepril Hydrochloride 5 mg / 10 mg capsule
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-756.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
| Lupin Limited | Pithampur, India | Makes it and packages it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Recalls
- Jul 2, 2025 · Class II · Lupin Pharmaceuticals Inc.
Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
Lots: Lot GB01616, expiration 2/28/2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Amlodipine and Benazeprilat: every company that makes it
- Form
- capsule
- Strength
- 5 mg / 10 mg
- Approval
- ANDA ANDA078466
- On the market since
- Feb 5, 2010
- Package NDCs
68151-1364-0- Official label
- DailyMed (National Library of Medicine), updated Jul 6, 2017
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