APPLICATION
ANDA213672
TYPE
ANDA
ORIGINAL APPROVAL
2023-07-24
LATEST ACTION
2025-03-26
ROUTE
SUBCUTANEOUS
DOSAGE FORM
SOLUTION
MARKETING STATUS
Prescription
Products
PLERIXAFORPrescription
PLERIXAFOR 24MG/1.2ML (20MG/ML) · SOLUTION · SUBCUTANEOUS
Approval history
2025-03-26Labeling · Supplement 1 · standardAP
2023-07-24UNKNOWN · Original · standardAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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