672 672 (Diltiazem Hydrochloride Extended Release 300 mg)

Pill with imprint 672 672 is Purple / White, Capsule-shape and has been identified as Diltiazem Hydrochloride Extended Release 300 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 300 mg is not a controlled substance under the Controlled Substances Act (CSA).

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Diltiazem Hydrochloride Extended Release

Imprint

672 672

Strength

300 mg

Color

Purple / White

Size

24.00 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)

47335-0672

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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