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FDA ANDA · ANDA076151

DILT-CD

Sponsor: APOTEX

APPLICATION
ANDA076151
TYPE
ANDA
ORIGINAL APPROVAL
2004-05-20
LATEST ACTION
2025-07-10
ROUTE
ORAL
DOSAGE FORM
CAPSULE, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

DILT-CDDiscontinued
DILTIAZEM HYDROCHLORIDE 300MG · CAPSULE, EXTENDED RELEASE · ORAL
DILT-CDDiscontinued
DILTIAZEM HYDROCHLORIDE 180MG · CAPSULE, EXTENDED RELEASE · ORAL
DILT-CDDiscontinued
DILTIAZEM HYDROCHLORIDE 240MG · CAPSULE, EXTENDED RELEASE · ORAL
DILT-CDDiscontinued
DILTIAZEM HYDROCHLORIDE 120MG · CAPSULE, EXTENDED RELEASE · ORAL

Approval history

2025-07-10Labeling · Supplement 17 · standardAP
2025-07-10Labeling · Supplement 16 · standardAP
2015-06-22Labeling · Supplement 10 · standardAP
2012-02-28Labeling · Supplement 9AP
2004-05-20OriginalReviewAP
VIEW ON DRUGS@FDA ↗

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