All FDA drug approvals

FDA approval · Drugs@FDA

NUCYNTA ERtapentadol hydrochloride

NDA200533 ·

FDA approved the original new drug application for NUCYNTA ER on August 25, 2011, sponsored by COLLEGIUM PHARM INC. FDA has approved 2 efficacy supplements on the application since, the most recent on June 14, 2024.

Application
NDA200533
Sponsor
COLLEGIUM PHARM INC
Original approval
Review
standard review
Submission class
Type 3 - New Dosage Form
Active ingredient
tapentadol hydrochloride

Products under this application

Ingredient and strengthFormRouteMarketing status
tapentadol hydrochloride EQ 200MG BASETABLET, EXTENDED RELEASEORALPrescription
tapentadol hydrochloride EQ 100MG BASETABLET, EXTENDED RELEASEORALPrescription
tapentadol hydrochloride EQ 250MG BASETABLET, EXTENDED RELEASEORALPrescription
tapentadol hydrochloride EQ 150MG BASETABLET, EXTENDED RELEASEORALPrescription
tapentadol hydrochloride EQ 50MG BASETABLET, EXTENDED RELEASEORALPrescription

Approved efficacy supplements

An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.

ApprovedSupplementReview
S-1standard
S-29priority

FDA records other approved supplements on this application, by the class code it assigns them: REMS 10 · Labeling 7 · Manufacturing (CMC) 1. Those are changes to the label or to how the drug is made rather than new clinical evidence, so they are counted here and not listed.

Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.

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