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"71335-2922-1" National Drug Code (NDC)

Mexiletine Hydrochloride 100 CAPSULE in 1 BOTTLE (71335-2922-1)
(Bryant Ranch Prepack)

NDC Code71335-2922-1
Package Description100 CAPSULE in 1 BOTTLE (71335-2922-1)
Product NDC71335-2922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMexiletine Hydrochloride
Non-Proprietary NameMexiletine Hydrochloride
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20211129
Marketing Category NameANDA
Application NumberANDA214089
ManufacturerBryant Ranch Prepack
Substance NameMEXILETINE HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAntiarrhythmic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2922-1





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