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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; diabetic peripheral neuropathy; arrhythmia; myotonia congenita 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 Front
Mexiletine hydrochloride 200 mg N 740 200 Back

Mexiletine Hydrochloride

Imprint:
N 740 200
Strength:
200 mg
Color:
Orange
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.

Other Labelers / Repackagers:

NDC CodeLabeler / Repackager
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.

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