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FDA ANDA · ANDA061894

ILOSONE

Sponsor: LILLY

APPLICATION
ANDA061894
TYPE
ANDA
ORIGINAL APPROVAL
1975-01-07
LATEST ACTION
1997-07-22
ROUTE
ORAL
DOSAGE FORM
SUSPENSION/DROPS, SUSPENSION
MARKETING STATUS
Discontinued

Products

ILOSONEDiscontinued
ERYTHROMYCIN ESTOLATE EQ 100MG BASE/ML · SUSPENSION/DROPS · ORAL
ILOSONEDiscontinued
ERYTHROMYCIN ESTOLATE EQ 125MG BASE/5ML · SUSPENSION · ORAL
ILOSONEDiscontinued
ERYTHROMYCIN ESTOLATE EQ 250MG BASE/5ML · SUSPENSION · ORAL

Approval history

1997-07-22Labeling · Supplement 19AP
1992-01-27Manufacturing (CMC) · Supplement 14AP
1991-11-13Labeling · Supplement 9AP
1991-11-13Labeling · Supplement 13AP
1991-09-05Labeling · Supplement 10AP
1991-01-14Labeling · Supplement 12AP
1990-04-16Labeling · Supplement 11AP
1990-04-10Manufacturing (CMC) · Supplement 8AP
1990-04-10Manufacturing (CMC) · Supplement 6AP
1975-01-07OriginalAP
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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