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N 740 200 (Mexiletine 200 mg)

This 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 diabetic peripheral neuropathy; myotonia congenita; 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 Substance Act (CSA).

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

N 740 200
200 mg
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
titanium dioxide
ferrosoferric oxide
D&C Yellow No. 10
FD&C Blue No. 1
FD&C Blue No. 2
FD&C Red No. 40
isopropyl alcohol
butyl alcohol
propylene glycol
Note: Inactive ingredients may vary.

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Other Labelers / Repackagers:
NDC CodeLabeler / Repackager
42291-0625 AvKare, Inc.

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