Drugplain

NDC 70756-315-30

telmisartan and hydrochlorothiazide 12.5 mg/1

telmisartan and hydrochlorothiazide · TABLET

No Recall History

telmisartan and hydrochlorothiazide is a tablet containing telmisartan and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by Lifestar Pharma LLC.

Key Facts

Brand Name
telmisartan and hydrochlorothiazide
Generic Name
telmisartan and hydrochlorothiazide
NDC Code (Package)
70756-315-30
NDC Code (Product)
70756-315
Manufacturer
Lifestar Pharma LLC
Strength
12.5 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA218406
Drug Class
Thiazide Diuretic [EPC]; Angiotensin 2 Receptor Blocker [EPC]
Marketing Start
12/25/2025

Recall History

No Recall History

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