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FDA ANDA · ANDA204532

OLOPATADINE HYDROCHLORIDE

Sponsor: SCIEGEN PHARMS

APPLICATION
ANDA204532
TYPE
ANDA
ORIGINAL APPROVAL
2017-01-10
LATEST ACTION
2021-06-23
ROUTE
OPHTHALMIC
DOSAGE FORM
SOLUTION/DROPS
MARKETING STATUS
Discontinued

Products

OLOPATADINE HYDROCHLORIDEDiscontinued
OLOPATADINE HYDROCHLORIDE EQ 0.1% BASE · SOLUTION/DROPS · OPHTHALMIC

Approval history

2021-06-23Labeling · Supplement 4 · standardAP
2017-01-10UNKNOWN · OriginalAP
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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