PlainRecalls
FDA Drug Low Class III Terminated

Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10

Reported: May 2, 2018 Initiated: April 23, 2018 #D-0715-2018

Product Description

Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10

Reason for Recall

Failed Dissolution Specifications. High dissolution results were obtained during stability testing.

Details

Units Affected
7656 cartons
Distribution
Nationwide with the US
Location
Concord, NC

Frequently Asked Questions

What product was recalled?
Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10. Recalled by Mckesson Packaging Services. Units affected: 7656 cartons.
Why was this product recalled?
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 2, 2018. Severity: Low. Recall number: D-0715-2018.