All FDA drug approvals

FDA approval · Drugs@FDA

PERTZYEpancrelipase (amylase, lipase, protease)

BLA022175 ·

FDA approved the original biologics license application for PERTZYE on May 17, 2012, sponsored by DIGESTIVE CARE INC. FDA’s record shows no approved efficacy supplement on the application since.

Application
BLA022175
Sponsor
DIGESTIVE CARE INC
Original approval
Review
standard review
Submission class
Type 7 - Drug Already Marketed without Approved NDA
Active ingredient
pancrelipase (amylase, lipase, protease)

Products under this application

Ingredient and strengthFormRouteMarketing status
pancrelipase (amylase 90,750USP UNITS; lipase 24,000USP UNITS; protease) 86,250USP UNITSCAPSULE, DELAYED RELEASEORALPrescription
pancrelipase (amylase 60,500USP UNITS; lipase 16,000USP UNITS; protease) 57,500USP UNITSCAPSULE, DELAYED RELEASEORALPrescription
pancrelipase (amylase 15,125USP UNITS; lipase 4,000USP UNITS; protease) 14,375USP UNITSCAPSULE, DELAYED RELEASEORALPrescription
pancrelipase (amylase 30,250USP UNITS; lipase 8,000USP UNITS; protease) 28,750USP UNITSCAPSULE, DELAYED 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.

FDA’s record shows no approved efficacy supplement on this application.

FDA records other approved supplements on this application, by the class code it assigns them: Labeling 4 · Manufacturing (CMC) 2. 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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