NDC 53489-217
Clonidine Hydrochloride 0.3 mg tablet
On the label: Mutual Pharmaceutical Company, Inc..
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 #: 6676701 and 6676801, exp 1/17
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
- 0.3 mg
- Approval
- ANDA ANDA070923
- On the market since
- Sep 4, 1987
- Package NDCs
53489-217-01- Official label
- DailyMed (National Library of Medicine), updated Sep 25, 2014
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