NDC 50436-3526

Clonidine Hydrochloride 0.3 mg tablet

On the label: Unit Dose Services. It's a repackaged product: Unit Dose Services rebottles it from Mutual Pharmaceutical Company, Inc.'s NDC 53489-217.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Mutual Pharmaceutical Company, Inc. uses for other drugs.

Repackaging site

• Unit Dose Services, · repackages it and relabels it

Recalls

• Jul 9, 2015 · Class II · Terminated
  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 #: 6676701 and 6676801, exp 1/17

Product details

Generic drug

Clonidine: see every company that makes it

Form

tablet

Strength

0.3 mg

Approval

ANDA ANDA070923

On the market since

Sep 4, 1987

Package NDCs

50436-3526-1 50436-3526-3

Official label

DailyMed (National Library of Medicine), updated May 30, 2019

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