NDC 71335-3095
Amlodipine Besylate and Benazepril Hydrochloride 5 mg / 20 mg capsule
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-459.
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
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels 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, oral
- Strength
- 5 mg / 20 mg
- Approval
- ANDA ANDA078466
- On the market since
- Aug 1, 2018
- Package NDCs
71335-3095-171335-3095-2- Official label
- DailyMed (National Library of Medicine), updated Feb 24, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?