NDC 70934-705
bisoprolol fumarate and hydrochlorothiazide 5 mg / 6.25 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-188.
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
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages 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
- 5 mg / 6.25 mg
- Approval
- ANDA ANDA079106
- On the market since
- May 13, 2020
- Package NDCs
70934-705-90- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?