NDC 0187-2050-90
Cardizem LA 420 mg/1
Diltiazem Hydrochloride · TABLET, EXTENDED RELEASE
Cardizem LA is a tablet, extended release containing diltiazem hydrochloride at a strength of 420 mg/1. Manufactured by Bausch Health US LLC.
Key Facts
- Brand Name
- Cardizem LA
- Generic Name
- Diltiazem Hydrochloride
- NDC Code (Package)
0187-2050-90- NDC Code (Product)
0187-2050- Manufacturer
- Bausch Health US LLC
- Strength
- 420 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA021392
- Marketing Start
- 12/25/2010
Recall History
No Recall HistoryView Full Drug Page
Cardizem LA — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.