Candesartan Cilexetil and Hydrochlorothiazide 32 mg / 12.5 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 2, 2020 · Class III · Mylan Pharmaceuticals Inc.
  Out-of-specification organic impurity results obtained during routine stability testing.
  Lots: Lot #: a) 8095666, Exp. Date July 2021 b) 3104664, Exp. Date July 2021

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

Product details

Generic drug

Candesartan and Hydrochlorothiazide: every company that makes it

Form

tablet

Strength

32 mg / 12.5 mg

Approval

ANDA ANDA090704

On the market since

Dec 4, 2012

Package NDCs

0378-3002-77

Official label

DailyMed (National Library of Medicine), updated Aug 15, 2020

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