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FDA ANDA · ANDA206306

OLOPATADINE

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APPLICATION
ANDA206306
TYPE
ANDA
ORIGINAL APPROVAL
2015-12-07
LATEST ACTION
2024-04-09
ROUTE
OPHTHALMIC
DOSAGE FORM
SOLUTION/DROPS
MARKETING STATUS
Over-the-counter

Products

OLOPATADINE HYDROCHLORIDEOver-the-counter
OLOPATADINE HYDROCHLORIDE EQ 0.1% BASE · SOLUTION/DROPS · OPHTHALMIC

Approval history

2024-04-09Labeling · Supplement 11 · standardAP
2015-12-07UNKNOWN · Original · standardLetterAP
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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