NDC 0093-3242-01
bisoprolol fumarate and hydrochlorothiazide 5 mg/1
bisoprolol fumarate and hydrochlorothiazide · TABLET, FILM COATED
bisoprolol fumarate and hydrochlorothiazide is a tablet, film coated containing bisoprolol fumarate and hydrochlorothiazide at a strength of 5 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- bisoprolol fumarate and hydrochlorothiazide
- Generic Name
- bisoprolol fumarate and hydrochlorothiazide
- NDC Code (Package)
0093-3242-01- NDC Code (Product)
0093-3242- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA020186
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 08/07/2019
Recall History
No Recall HistoryView Full Drug Page
bisoprolol fumarate and hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.