NDC 66267-062
clonidine hydrochloride 0.2 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-136.
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 Unichem Pharmaceuticals (USA), Inc. names for other drugs.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Recalls
- Sep 19, 2022 · Class III · Unichem Pharmaceuticals Usa Inc
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Lots: Lot # GCLH22005, exp. date 02/29/2024 - May 26, 2020 · Class III · Unichem Pharmaceuticals Usa Inc
Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container.
Lots: Lot #: GCLL19034, GCLL19035, GCLL19036, Exp. 4/30/2021; GCLL19044, Exp. 6/30/2021 - Jan 29, 2020 · Class III · Unichem Pharmaceuticals Usa Inc
Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container label.
Lots: Lot Numbers: GCLL18108, GCLL18109, GCLL18110 - EXP 10/31/2020; GCLL19003 EXP 12/31/2020
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 ANDA078895
- On the market since
- Sep 21, 2009
- Package NDCs
66267-062-3066267-062-6066267-062-90- Official label
- DailyMed (National Library of Medicine), updated Jan 11, 2021
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