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FDA NDA · NDA200533
TAPENTADOL
tapentadol hydrochloride
Sponsor: COLLEGIUM PHARM INC
APPLICATION
NDA200533
TYPE
NDA
ORIGINAL APPROVAL
2011-08-25
LATEST ACTION
2026-06-18
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Prescription
Products
NUCYNTA ER · ReferencePrescription
TAPENTADOL HYDROCHLORIDE EQ 200MG BASE · TABLET, EXTENDED RELEASE · ORAL
NUCYNTA ER · ReferencePrescription
TAPENTADOL HYDROCHLORIDE EQ 100MG BASE · TABLET, EXTENDED RELEASE · ORAL
NUCYNTA ER · ReferencePrescription
TAPENTADOL HYDROCHLORIDE EQ 250MG BASE · TABLET, EXTENDED RELEASE · ORAL
NUCYNTA ER · ReferencePrescription
TAPENTADOL HYDROCHLORIDE EQ 150MG BASE · TABLET, EXTENDED RELEASE · ORAL
NUCYNTA ER · ReferencePrescription
TAPENTADOL HYDROCHLORIDE EQ 50MG BASE · TABLET, EXTENDED RELEASE · ORAL
Approval history
2014-01-16Manufacturing (CMC) · Supplement 7 · standardAP
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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