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FDA ANDA · ANDA211021

ICATIBANT

Sponsor: JIANGSU HANSOH PHARM

APPLICATION
ANDA211021
TYPE
ANDA
ORIGINAL APPROVAL
2020-03-09
LATEST ACTION
2025-01-03
ROUTE
SUBCUTANEOUS
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Prescription

Products

ICATIBANT ACETATEPrescription
ICATIBANT ACETATE EQ 30MG BASE/3ML (EQ 10MG BASE/ML) · INJECTABLE · SUBCUTANEOUS

Approval history

2025-01-03Labeling · Supplement 12 · standardAP
2023-11-28Labeling · Supplement 6 · standardAP
2020-09-25Labeling · Supplement 3 · standardAP
2020-03-09UNKNOWN · Original · standardAP
VIEW ON DRUGS@FDA ↗

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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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