Andrx 700 360 mg (Diltiazem Hydrochloride Extended-Release 360 mg)
Pill with imprint Andrx 700 360 mg is Blue, Capsule-shape and has been identified as Diltiazem Hydrochloride Extended-Release 360 mg. It is supplied by PuraCap Laboratories, LLC.
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 360 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for Andrx 700 360 mg
Diltiazem Hydrochloride Extended-Release
- Imprint
- Andrx 700 360 mg
- Strength
- 360 mg
- Color
- Blue
- Size
- 23.00 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
- PuraCap Laboratories, LLC
- National Drug Code (NDC)
- 24658-0345
- Inactive Ingredients
-
ferrosoferric oxide,
corn starch,
ethylcellulose (10 mPa.s),
D&C Yellow No. 10,
FD&C Blue No. 1,
FD&C Blue No. 2,
FD&C Red No. 40,
gelatin,
hypromellose 2910 (5 mPa.s),
magnesium stearate,
nonoxynol-100,
shellac,
polysorbate 80,
povidone,
propylene glycol,
sucrose,
magnesium silicate,
titanium dioxide,
aluminum oxide
Note: Inactive ingredients may vary.
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- During pregnancy or Breastfeeding
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- Drug class: calcium channel blocking agents
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Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.