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Mexiletine Hydrochloride - 0093-8741-01 - (Mexiletine Hydrochloride)

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Drug Information of Mexiletine Hydrochloride

Product NDC: 0093-8741
Proprietary Name: Mexiletine Hydrochloride
Non Proprietary Name: Mexiletine Hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   Mexiletine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Mexiletine Hydrochloride

Product NDC: 0093-8741
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074377
Marketing Category: ANDA
Start Marketing Date: 19950605

Package Information of Mexiletine Hydrochloride

Package NDC: 0093-8741-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-8741-01)

NDC Information of Mexiletine Hydrochloride

NDC Code 0093-8741-01
Proprietary Name Mexiletine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0093-8741-01)
Product NDC 0093-8741
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mexiletine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950605
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name MEXILETINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Mexiletine Hydrochloride


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