Mckesson Packaging Services recalls Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ri…
- Recall date
- April 23, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0716-2018
- FDA classification
- Class III
- Brand / firm
- Mckesson Packaging Services
- Sold / distributed
- Nationwide with the US
Why it was recalled
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-016-10
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