NDC 63187-202
Clonidine Hydrochloride 0.1 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Mutual Pharmaceutical Company, Inc.'s NDC 53489-215.
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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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) 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, oral
- Strength
- 0.1 mg
- Approval
- ANDA ANDA070925
- On the market since
- Sep 4, 1987
- Package NDCs
63187-202-3063187-202-6063187-202-90- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?