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FDA ANDA · ANDA209582

DOXYCYCLINE

Sponsor: ZYDUS PHARMS

APPLICATION
ANDA209582
TYPE
ANDA
ORIGINAL APPROVAL
2017-09-28
LATEST ACTION
2026-01-17
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

DOXYCYCLINEPrescription
DOXYCYCLINE EQ 100MG BASE · TABLET · ORAL
DOXYCYCLINEPrescription
DOXYCYCLINE EQ 50MG BASE · TABLET · ORAL
DOXYCYCLINEPrescription
DOXYCYCLINE EQ 150MG BASE · TABLET · ORAL
DOXYCYCLINEPrescription
DOXYCYCLINE EQ 75MG BASE · TABLET · ORAL

Approval history

2026-01-17Labeling · Supplement 1 · standardAP
2026-01-17Labeling · Supplement 8 · standardAP
2026-01-17Labeling · Supplement 6 · standardAP
2017-09-28UNKNOWN · 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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