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N 740 200 (Mexiletine 200 mg)

Pill imprint N 740 200 has been identified as Mexiletine hydrochloride 200 mg.

Mexiletine is used in the treatment of myotonia congenita; ventricular tachycardia; diabetic peripheral neuropathy; 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
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
Manufacturer:
Teva Pharmaceuticals USA
National Drug Code (NDC):
00093-8740
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
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
42291-0625 AvKare, Inc.
55045-3651 Dispensing Solutions Inc. (repackager)

Note: Inactive ingredients may vary.

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