NDC 54868-2149
Cardizem CD 240 mg capsule
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Bausch Health US, LLC's NDC 0187-0797.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch Health Companies Inc. | Steinbach, Canada | Makes it | No problems foundMay 19, 2023 · 6 inspections |
Recalls
- Jan 30, 2019 · Class III · Valeant Pharmaceuticals North America LLC
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Lots: Lots: a) 18J023P, Exp 08/2020; b) 18J021P, Exp 08/2020 - Jan 30, 2019 · Class III · Valeant Pharmaceuticals North America LLC
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Lots: Lots: a) 18J018P, Exp 08/2020; b) 18J029P, Exp 08/2020 - Jan 30, 2019 · Class III · Valeant Pharmaceuticals North America LLC
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Lots: Lots: a) 18J019P, Exp 08/2020; b) 18J028P, Exp 08/2020 - Jan 30, 2019 · Class III · Valeant Pharmaceuticals North America LLC
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Lots: Lots: a)18J020P, Exp 08/2020; b) 18J034P, Exp 08/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- capsule
- Strength
- 240 mg
- Approval
- NDA NDA020062
- On the market since
- Jun 16, 1993
- Package NDCs
54868-2149-0- Official label
- DailyMed (National Library of Medicine), updated Mar 26, 2012
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