Catapres (clonidine hydrochloride, USP) 0.3 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0011-01
Reported: November 4, 2020 Initiated: October 5, 2020 #D-0053-2021
Product Description
Catapres (clonidine hydrochloride, USP) 0.3 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0011-01
Reason for Recall
An extraneous peak was observed for dissolution testing.
Details
- Recalling Firm
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Units Affected
- N/A
- Distribution
- Distributed Nationwide in the USA and Puerto Rico
- Location
- Ridgefield, CT
Frequently Asked Questions
What product was recalled? ▼
Catapres (clonidine hydrochloride, USP) 0.3 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0011-01. Recalled by Boehringer Ingelheim Pharmaceuticals, Inc.. Units affected: N/A.
Why was this product recalled? ▼
An extraneous peak was observed for dissolution testing.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 4, 2020. Severity: Moderate. Recall number: D-0053-2021.
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