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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More about diltiazem
- Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Patient Tips
- Drug Images
- Drug Interactions
- Compare Alternatives
- Support Group
- Pricing & Coupons
- En Español
- 138 Reviews
- Drug class: calcium channel blocking agents
Consumer resources
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Professional resources
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
