NDC 72789-502
Amlodipine Besylate and Benazepril Hydrochloride 10 mg / 20 mg capsule
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-472.
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
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, 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, oral
- Strength
- 10 mg / 20 mg
- Approval
- ANDA ANDA078466
- On the market since
- Aug 1, 2018
- Package NDCs
72789-502-90- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2026
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