N 739 150 (Mexiletine 150 mg)

Pill imprint N 739 150 has been identified as Mexiletine hydrochloride 150 mg.

Mexiletine is used in the treatment of ventricular tachycardia; diabetic peripheral neuropathy; myotonia congenita; arrhythmia and belongs to the drug class group I antiarrhythmics. Risk cannot be ruled out during pregnancy. Mexiletine 150 mg is not subject to the Controlled Substances Act.

See also related documents.

Images for N 739 150 (Mexiletine 150 mg)

Mexiletine hydrochloride 150 mg N 739 150
Mexiletine hydrochloride 150 mg N 739 150 Front
Mexiletine hydrochloride 150 mg N 739 150 Back
Mexiletine hydrochloride
Imprint:
N 739
150
Strength:
150 mg
Color:
Tan / Orange
Size:
18.00 mm
Shape:
Capsule-shape
Availability:
Prescription only
Drug Class:
Group I antiarrhythmics
Pregnancy Category:
C - Risk cannot be ruled out
CSA Schedule:
N - Not a controlled drug
Manufacturer:
Teva Pharmaceuticals USA
National Drug Code (NDC):
00093-8739
Inactive Ingredients:
silicon dioxide
magnesium stearate
corn starch
FD&C Yellow No. 6
gelatin
titanium dioxide
D&C Red No. 28
FD&C Blue No. 1
ammonia
ferrosoferric oxide
D&C Yellow No. 10
alcohol
FD&C Blue No. 2
FD&C Red No. 40
isopropyl alcohol
butyl alcohol
propylene glycol
shellac
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
55045-3634 Dispensing Solutions Inc. (repackager)
49999-0916 Lake Erie Medical and Surgical Supply (repackager)

Note: Inactive ingredients may vary.

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