NDC 73377-114 - Bromhexine HCl

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 73377-114
Package NDCs from labels: 73377-114-01
Manufacturer: AX Pharmaceutical Corp
Effective date: 2021-02-23
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Bromhexine HCl - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2021-02-23	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73377-114-01	Bromhexine HCl	500 g in 1 JAR	POWDER	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73377-114	BROMHEXINE HCL POWDER [AX PHARMACEUTICAL CORP]	1	1 package rows	20210224_bd2bbcf5-6ed8-448f-b6c6-82e2bdfe93a3.zip

Reported adverse events (FAERS/openFDA)#

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