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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 062324

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NDA 062324 describes KANAMYCIN, which is a drug marketed by Hikma, Abraxis Pharm, Fresenius Kabi Usa, Intl Medication, Loch, Pharmafair, Solopak, Warner Chilcott, and Watson Labs, and is included in thirteen NDAs. Additional details are available on the KANAMYCIN profile page.

The generic ingredient in KANAMYCIN is kanamycin sulfate. There are five drug master file entries for this compound. Additional details are available on the kanamycin sulfate profile page.

Summary for 062324

Tradename:	KANAMYCIN
Applicant:	Hikma
Ingredient:	kanamycin sulfate
Patents:	0

Medical Subject Heading (MeSH) Categories for 062324

Anti-Bacterial Agents
Protein Synthesis Inhibitors

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 75MG BASE/2ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 500MG BASE/2ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 1GM BASE/3ML
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	No

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