NDC 10544-174
bisoprolol fumarate and hydrochlorothiazide 10 mg / 6.25 mg tablet
On the label: Blenheim Pharmacal, Inc.. It's repackaged: Blenheim Pharmacal, Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-189.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Unichem Pharmaceuticals (USA), Inc. names for other drugs.
Repackaging site
- Blenheim Pharmacal, Inc., North Blenheim, New York, United States · repackages it and relabels it
Recalls
- Jan 21, 2026 · Class II · Unichem Pharmaceuticals USA Inc.
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
Lots: Lot # GBHL24005A, Exp Date: 09/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Bisoprolol and Hydrochlorothiazide: every company that makes it
- Form
- tablet
- Strength
- 10 mg / 6.25 mg
- Approval
- ANDA ANDA079106
- On the market since
- Nov 15, 2013
- Package NDCs
10544-174-90- Official label
- DailyMed (National Library of Medicine), updated Feb 12, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?