Telmisartan and Amlodipine 5 mg / 80 mg tablet

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Mylan Pharmaceuticals Inc. names for other drugs.

Recalls

• Oct 1, 2026 · Class III · Viatris, Inc.
  Superpotent Drug: potential for the Telmisartan content in these lots to exceed specifications
  Lots: Lot # 3228113, 3228114, 3228115, Exp Date: Oct 31, 2026; Lot # 3228120, 3228121, Exp Date: Nov 30, 2026.

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Amlodipine and Telmisartan: every company that makes it

Form

tablet, oral

Strength

5 mg / 80 mg

Approval

ANDA ANDA202516

On the market since

Sep 19, 2014

Package NDCs

0378-1077-93

Official label

DailyMed (National Library of Medicine), updated Nov 14, 2018

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?