669 669 (Diltiazem Extended Release 120 mg)

This pill with imprint "669 669" is Purple, Capsule-shape and has been identified as Diltiazem hydrochloride extended release 120 mg. It is manufactured by Sun Pharmaceutical Industries Inc..

Diltiazem is used in the treatment of atrial fibrillation; supraventricular tachycardia; atrial flutter; high blood pressure; raynaud's syndrome (and more), and belongs to the drug classes calcium channel blocking agents, group IV antiarrhythmics. Risk cannot be ruled out during pregnancy. Diltiazem 120 mg is not a controlled substance under the Controlled Substance Act (CSA).

Diltiazem hydrochloride extended release

Imprint:

669 669

Strength:

120 mg

Color:

Purple

Shape:

Capsule-shape

Availability:

Prescription only

Drug Class:

Calcium channel blocking agents
Group IV antiarrhythmics

Pregnancy Category:

C - Risk cannot be ruled out

CSA Schedule:

Not a controlled drug

Manufacturer:

Sun Pharmaceutical Industries Inc.

National Drug Code (NDC):

47335-0669

Inactive Ingredients:

hypromellose 2910 (5 mPa.s)
magnesium silicate
ethylcelluloses
triethyl citrate
gelatin
titanium dioxide
sodium lauryl sulfate
FD&C Blue No. 1
FD&C Red No. 3

Note: Inactive ingredients may vary.

More info Print Imprint Search

Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 2017 Drugs.com, National Library of Medicine, Truven Health Analytics and Cerner Multum, Inc. All Rights Reserved.