NDC 55111-339
Amlodipine Besylate and Benazepril Hydrochloride 5 mg / 10 mg capsule
On the label: Dr.Reddy's Laboratories Ltd..
Where it's 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 |
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
- 5 mg / 10 mg
- Approval
- ANDA ANDA077183
- On the market since
- Apr 19, 2010
- Package NDCs
55111-339-0155111-339-0555111-339-30- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2022
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