FDA.reportPublic FDA data

Bromhexine HCl

Manufacturer
AX Pharmaceutical Corp
Effective date
2021-02-23
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:53

Label at a glance#

ProductBromhexine HCl
Active ingredientBROMHEXINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Bromhexine HCl

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-114-01Bromhexine HCl500 g in 1 JARPOWDER5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-114BROMHEXINE HCL POWDER [AX PHARMACEUTICAL CORP]11 package rows20210224_bd2bbcf5-6ed8-448f-b6c6-82e2bdfe93a3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73377-11473377-114-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
BROMHEXINE HYDROCHLORIDEYC2ZOM3Z8VACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.