Drugplain

NDC 0555-0483-02

Amiloride Hydrochloride and Hydrochlorothiazide 5 mg/1

Amiloride Hydrochloride and Hydrochlorothiazide · TABLET

No Recall History

Amiloride Hydrochloride and Hydrochlorothiazide is a tablet containing amiloride hydrochloride and hydrochlorothiazide at a strength of 5 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..

Key Facts

Brand Name
Amiloride Hydrochloride and Hydrochlorothiazide
Generic Name
Amiloride Hydrochloride and Hydrochlorothiazide
NDC Code (Package)
0555-0483-02
NDC Code (Product)
0555-0483
Manufacturer
Teva Pharmaceuticals USA, Inc.
Strength
5 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA071111
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
12/01/1989

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.