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FDA ANDA · ANDA075401

TAZTIA XT

Sponsor: ACTAVIS LABS FL INC

APPLICATION
ANDA075401
TYPE
ANDA
ORIGINAL APPROVAL
2003-04-10
LATEST ACTION
2011-11-30
ROUTE
ORAL
DOSAGE FORM
CAPSULE, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

TAZTIA XTDiscontinued
DILTIAZEM HYDROCHLORIDE 360MG · CAPSULE, EXTENDED RELEASE · ORAL
TAZTIA XTDiscontinued
DILTIAZEM HYDROCHLORIDE 240MG · CAPSULE, EXTENDED RELEASE · ORAL
TAZTIA XTDiscontinued
DILTIAZEM HYDROCHLORIDE 120MG · CAPSULE, EXTENDED RELEASE · ORAL
TAZTIA XTDiscontinued
DILTIAZEM HYDROCHLORIDE 300MG · CAPSULE, EXTENDED RELEASE · ORAL
TAZTIA XTDiscontinued
DILTIAZEM HYDROCHLORIDE 180MG · CAPSULE, EXTENDED RELEASE · ORAL

Approval history

2011-11-30Labeling · Supplement 20AP
2008-07-29Labeling · Supplement 11AP
2003-04-10OriginalLetterAP
VIEW ON DRUGS@FDA ↗

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