Last Updated: September 24, 2026

Details for New Drug Application (NDA): 062933

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NDA 062933 describes VANCOMYCIN HYDROCHLORIDE, which is a drug marketed by Fresenius Kabi Usa, Lupin, Orient Pharma Co Ltd, Pai Holdings, Strides Pharma, Watson Labs, Alkem Labs Ltd, Amneal, Aurobindo Pharma, Aspiro, Avet Lifesciences, Eugia Pharma, Eurofarma, Gland, Hainan Poly, Hikma, Hikma Pharms, Hospira, Hospira Inc, Knack, Meitheal, Mylan Labs Ltd, Plano Pharms, Sagent Pharms, Teva Pharms Usa, Xellia Pharms Aps, Samson Medcl, Steriscience, Zhejiang Novus Pharm, and Baxter Hlthcare, and is included in fifty-five NDAs. It is available from thirty-two suppliers. Additional details are available on the VANCOMYCIN HYDROCHLORIDE profile page.

The generic ingredient in VANCOMYCIN HYDROCHLORIDE is vancomycin hydrochloride. There is one drug master file entry for this compound. Thirty-seven suppliers are listed for this compound. Additional details are available on the vancomycin hydrochloride profile page.

Summary for 062933

Tradename:	VANCOMYCIN HYDROCHLORIDE
Applicant:	Hospira
Ingredient:	vancomycin hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 062933

Anti-Bacterial Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	INJECTABLE;INJECTION			Strength	EQ 1GM BASE/VIAL
Approval Date:	Oct 29, 1992	TE:	AP	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	INJECTABLE;INJECTION			Strength	EQ 750MG BASE/VIAL
Approval Date:	May 27, 2009	TE:	AP	RLD:	No

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