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Last Updated: November 24, 2024

Details for New Drug Application (NDA): 214352


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NDA 214352 describes MEXILETINE HYDROCHLORIDE, which is a drug marketed by Ani Pharms, Annora Pharma, Crossmedika Sa, Leading, Novast Labs, Senores Pharms, Teva, Watson Labs, and Zenara, and is included in ten NDAs. It is available from fourteen suppliers. Additional details are available on the MEXILETINE HYDROCHLORIDE profile page.

The generic ingredient in MEXILETINE HYDROCHLORIDE is mexiletine hydrochloride. There are five drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the mexiletine hydrochloride profile page.
Summary for 214352
Tradename:MEXILETINE HYDROCHLORIDE
Applicant:Novast Labs
Ingredient:mexiletine hydrochloride
Patents:0
Pharmacology for NDA: 214352
Medical Subject Heading (MeSH) Categories for 214352
Suppliers and Packaging for NDA: 214352
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MEXILETINE HYDROCHLORIDE mexiletine hydrochloride CAPSULE;ORAL 214352 ANDA Ingenus Pharmaceuticals, LLC 50742-239 50742-239-01 100 CAPSULE in 1 BOTTLE (50742-239-01)
MEXILETINE HYDROCHLORIDE mexiletine hydrochloride CAPSULE;ORAL 214352 ANDA Ingenus Pharmaceuticals, LLC 50742-240 50742-240-01 100 CAPSULE in 1 BOTTLE (50742-240-01)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength150MG
Approval Date:Jan 25, 2021TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength200MG
Approval Date:Jan 25, 2021TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength250MG
Approval Date:Jan 25, 2021TE:ABRLD:No

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