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FDA ANDA · ANDA091607

TRAMADOL HYDROCHLORIDE

Sponsor: SUN PHARM

APPLICATION
ANDA091607
TYPE
ANDA
ORIGINAL APPROVAL
2011-12-30
LATEST ACTION
2026-06-18
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

TRAMADOL HYDROCHLORIDEDiscontinued
TRAMADOL HYDROCHLORIDE 200MG · TABLET, EXTENDED RELEASE · ORAL
TRAMADOL HYDROCHLORIDEDiscontinued
TRAMADOL HYDROCHLORIDE 300MG · TABLET, EXTENDED RELEASE · ORAL
TRAMADOL HYDROCHLORIDEDiscontinued
TRAMADOL HYDROCHLORIDE 100MG · TABLET, EXTENDED RELEASE · ORAL

Approval history

2026-06-18REMS · Supplement 37AP
2025-12-29Labeling · Supplement 36 · standardAP
2025-12-12Labeling · Supplement 32 · standardAP
2024-10-31REMS · Supplement 33AP
2023-12-15Labeling · Supplement 29 · standardAP
2023-12-15Labeling · Supplement 31 · standardAP
2021-09-10Labeling · Supplement 26 · standardAP
2021-03-04Labeling · Supplement 24 · standardAP
2019-10-11Labeling · Supplement 19 · standardAP
2018-09-21Labeling · Supplement 16 · standardAP
2018-09-18REMS · Supplement 14AP
2017-08-29Labeling · Supplement 12 · standardAP
2017-08-29Labeling · Supplement 11 · standardAP
2017-08-21Labeling · Supplement 10 · standardAP
2016-12-16Labeling · Supplement 9 · standardAP
2016-12-16Labeling · Supplement 7 · standardAP
2011-12-30OriginalReviewAP
VIEW ON DRUGS@FDA ↗

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