NDC 68462-879-01
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 GLENMARK PHARMACEUTICALS INC., USA.
Key Facts
- Brand Name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic Name
- Bisoprolol Fumarate and Hydrochlorothiazide
- NDC Code (Package)
68462-879-01- NDC Code (Product)
68462-879- Manufacturer
- GLENMARK PHARMACEUTICALS INC., USA
- Strength
- 5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA215995
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 01/26/2022
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.