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669 669 (Diltiazem Hydrochloride Extended Release 120 mg)

Pill with imprint 669 669 is Purple, Capsule-shape and has been identified as Diltiazem Hydrochloride Extended Release 120 mg. It is supplied by Sun Pharmaceutical Industries Inc..

Diltiazem is used in the treatment of atrial fibrillation; atrial flutter; angina pectoris prophylaxis; heart failure; high blood pressure 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 Substances Act (CSA).

Images for 669 669

Diltiazem Hydrochloride Extended Release

Imprint
669 669
Strength
120 mg
Color
Purple
Size
18.00 mm
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
Labeler / Supplier
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.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.