NDC 59651-679
Bisoprolol Fumarate and Hydrochlorothiazide 5 mg / 6.25 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Bisoprolol and Hydrochlorothiazide: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg / 6.25 mg
- Approval
- ANDA ANDA217922
- On the market since
- Jan 21, 2026
- Package NDCs
59651-679-0159651-679-0559651-679-30- Official label
- DailyMed (National Library of Medicine), updated Sep 18, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?