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; myotonia congenita; diabetic peripheral neuropathy; 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.
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Images for N 739 150 (Mexiletine 150 mg)
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
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
D&C Red No. 28
| NDC Code | Manufacturer / 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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Mexiletine hydrochloride is associated with the treatment of:
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