Clonidine Hydrochloride 0.1 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 Mutual Pharmaceutical Company, Inc. names for other drugs.

Recalls

• Jul 9, 2015 · Class II · Mutual Pharmaceutical Company, Inc.
  cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
  Lots: Lot #: a) 6624001 exp 2/16, 6630501 exp 3/16, 6669001 exp 12/16, 6676201 exp 1/17, 6680701 exp 2/17; b) 6624002, 6624201 exp 2/16, 6630601 exp 3/16, 6668901 exp 12/16, 6676001, 6676101 exp 1/17, 6679401, 6679501, exp 2/17

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

Product details

Generic drug

Clonidine: every company that makes it

Form

tablet

Strength

0.1 mg

Approval

ANDA ANDA070925

On the market since

Sep 4, 1987

Package NDCs

53489-215-01 53489-215-10

Official label

DailyMed (National Library of Medicine), updated Sep 25, 2014

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