Last Updated: May 10, 2026

Details for New Drug Application (NDA): 211901

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NDA 211901 describes PLERIXAFOR, which is a drug marketed by Amneal, Dr Reddys, Eugia Pharma, Gland, Hetero Labs Ltd Vi, Meitheal, MSN, Teva Pharms Usa Inc, and Zydus Pharms, and is included in nine NDAs. It is available from eleven suppliers. Additional details are available on the PLERIXAFOR profile page.

The generic ingredient in PLERIXAFOR is plerixafor. There are seven drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the plerixafor profile page.

Summary for 211901

Tradename:	PLERIXAFOR
Applicant:	Msn
Ingredient:	plerixafor
Patents:	0

Pharmacology for NDA: 211901

Physiological Effect	Increased Hematopoietic Stem Cell Mobilization

Suppliers and Packaging for NDA: 211901

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
PLERIXAFOR	plerixafor	SOLUTION;SUBCUTANEOUS	211901	ANDA	Bryant Ranch Prepack	72162-2642	72162-2642-2	1 VIAL, SINGLE-DOSE in 1 CARTON (72162-2642-2) / 1.2 mL in 1 VIAL, SINGLE-DOSE
PLERIXAFOR	plerixafor	SOLUTION;SUBCUTANEOUS	211901	ANDA	Novadoz Pharmaceuticals LLC	72205-249	72205-249-01	1 VIAL, SINGLE-DOSE in 1 CARTON (72205-249-01) / 1.2 mL in 1 VIAL, SINGLE-DOSE

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;SUBCUTANEOUS			Strength	24MG/1.2ML (20MG/ML)
Approval Date:	Jul 24, 2023	TE:	AP	RLD:	No

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