NDC 0093-3241
bisoprolol fumarate and hydrochlorothiazide 2.5 mg / 6.25 mg tablet, film coated
On the label: Teva Pharmaceuticals USA, Inc..
Where it's 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 1417295A
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, film coated, oral
- Strength
- 2.5 mg / 6.25 mg
- Approval
- NDA authorized generic NDA020186
- On the market since
- Aug 7, 2019
- Package NDCs
0093-3241-01- Official label
- DailyMed (National Library of Medicine), updated Aug 11, 2026
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