NDC 72789-131
Acarbose 25 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0140.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Recalls
- Apr 2, 2015 · Class II · Boehringer Ingelheim Roxane Inc
Subpotent Drug: The firm received an out of specification result for Assay (potency was below specification) at the 9 month stability time point.
Lots: a) Lot # 460073A Exp 04/2016 b) Lot # 460073B Exp 04/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acarbose: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA078470
- On the market since
- May 7, 2008
- Package NDCs
72789-131-0172789-131-3072789-131-6072789-131-90- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2026
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