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N 740 200 (Mexiletine Hydrochloride 200 mg)

Pill with imprint N 740 200 is Orange, Capsule-shape and has been identified as Mexiletine Hydrochloride 200 mg. It is supplied by Teva Pharmaceuticals USA.

Mexiletine is used in the treatment of ventricular tachycardia; arrhythmia and belongs to the drug class group I antiarrhythmics. Risk cannot be ruled out during pregnancy. Mexiletine 200 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for N 740 200

Mexiletine hydrochloride 200 mg N 740 200
Mexiletine hydrochloride 200 mg N 740 200
Mexiletine hydrochloride 200 mg N 740 200
Mexiletine hydrochloride 200 mg N 740 200 Front
Mexiletine hydrochloride 200 mg N 740 200 Back

Mexiletine Hydrochloride

Imprint
N 740 200
Strength
200 mg
Color
Orange
Size
19.00 mm
Shape
Capsule-shape
Availability
Prescription only
Drug Class
Group i antiarrhythmics
Pregnancy Category
C - Risk cannot be ruled out
CSA Schedule
Not a controlled drug
Labeler / Supplier
Teva Pharmaceuticals USA
Inactive Ingredients
silicon dioxide, magnesium stearate, corn starch, FD&C Yellow No. 6, gelatin, titanium dioxide, ammonia, ferrosoferric oxide, D&C Yellow No. 10, alcohol, FD&C Blue No. 1, FD&C Blue No. 2, FD&C Red No. 40, isopropyl alcohol, butyl alcohol, propylene glycol, shellac

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code Labeler / Repackager
00093-8740 Teva Pharmaceuticals USA, Inc.
42291-0625 AvKare, Inc.

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Further information

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