NDC 82868-041
Amlodipine Besylate and Benazepril Hydrochloride 10 mg / 20 mg capsule
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-341.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Apr 9, 2012 · Class II · Dr. Reddy's Laboratories, Inc.
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets.
Lots: C201293 Exp Date 08/2013
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, oral
- Strength
- 10 mg / 20 mg
- Approval
- ANDA ANDA077183
- On the market since
- Jan 19, 2024
- Package NDCs
82868-041-90- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
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