Drugplain

TIAZAC EXTENDED RELEASE 240 mg/1

diltiazem hydrochloride · CAPSULE, EXTENDED RELEASE · Bausch Health US, LLC

No Recall HistoryCurrently in Shortage
Plain English

TIAZAC EXTENDED RELEASE is a capsule, extended release containing diltiazem hydrochloride at 240 mg/1, taken oral. Manufactured by Bausch Health US, LLC.

Key Facts

Brand Name
TIAZAC EXTENDED RELEASE
Generic Name
diltiazem hydrochloride
NDC Code (Product)
0187-2614
Manufacturer
Bausch Health US, LLC
Strength
240 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
NDA020401
Marketing Start
08/20/2014

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

dyspnoea1,498 reports
pain1,294 reports
fatigue1,246 reports
fall1,148 reports
headache996 reports
diarrhoea989 reports
arthralgia962 reports
nausea957 reports
dizziness939 reports
drug ineffective908 reports

Frequently Asked Questions

What is TIAZAC EXTENDED RELEASE used for?

TIAZAC EXTENDED RELEASE contains diltiazem hydrochloride. It is a capsule, extended release taken oral. Consult your doctor for specific uses.

Is TIAZAC EXTENDED RELEASE a controlled substance?

TIAZAC EXTENDED RELEASE is not classified as a controlled substance by the DEA.

What is the generic name for TIAZAC EXTENDED RELEASE?

The generic name for TIAZAC EXTENDED RELEASE is diltiazem hydrochloride. There are 11 other brand versions of diltiazem hydrochloride.

What is the NDC code for TIAZAC EXTENDED RELEASE 240 mg/1?

The NDC (National Drug Code) for TIAZAC EXTENDED RELEASE 240 mg/1 is 0187-2614, listed by Bausch Health US, LLC.