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"0093-8739-01" National Drug Code (NDC)

Mexiletine Hydrochloride 100 CAPSULE in 1 BOTTLE (0093-8739-01)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-8739-01
Package Description100 CAPSULE in 1 BOTTLE (0093-8739-01)
Product NDC0093-8739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMexiletine Hydrochloride
Non-Proprietary NameMexiletine Hydrochloride
Dosage FormCAPSULE
UsageORAL
Start Marketing Date19950605
Marketing Category NameANDA
Application NumberANDA074377
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameMEXILETINE HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAntiarrhythmic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-8739-01





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