Mexiletine HCl
Mexiletine HCl
Approved
Approval ID
b635fe28-11a7-4ea4-85d5-54d8b3aa896f
Product Type
BULK INGREDIENT - ANIMAL DRUG
Effective Date
May 12, 2025
Manufacturers
FDA
AX Pharmaceutical Corp
DUNS: 204011316
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Mexiletine HCl
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code73377-323
Product Classification
G
Generic Name
Mexiletine HCl
Product Specifications
Route of AdministrationNOT APPLICABLE
Effective DateMay 12, 2025
FDA Product Classification
INGREDIENTS (1)
MEXILETINE HYDROCHLORIDEActive
Quantity: 1 g in 1 g
Code: 606D60IS38
Classification: ACTIB
Drug Labeling Information
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
LOINC: 51945-4Updated: 5/12/2025
Mexiletine HCl
