NDC 51138-018
Clonidine Hydrochloride 0.2 mg tablet
On the label: Med Health Pharma, LLC. It's repackaged: Med Health Pharma, LLC rebottles it from Mutual Pharmaceutical Company, Inc.'s NDC 53489-216.
Where the pills inside were 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.
Repackaging site
- Med Health Pharma, LLC, Location not on file · repackages it
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) 6643901, exp 5/16, 6677201, exp 1/17; b) 6677101, 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
- 0.2 mg
- Approval
- ANDA ANDA070924
- On the market since
- Jan 10, 2011
- Package NDCs
51138-018-30- Official label
- DailyMed (National Library of Medicine), updated Jun 22, 2012
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