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CREON (LIPASE)

ABBVIE · FDA-approved approved Under review Quality 10/100

CREON (generic name: LIPASE) is a Vitamin C [EPC] drug developed by ABBVIE. It is currently FDA-approved.

CREON is a medication that belongs to the class of hydrolytic enzymes, specifically targeting fatty acids. It is used to treat conditions such as pancreatic insufficiency, pancreatic cancer, and postprandial symptoms like bloating and belching.

At a glance

Generic nameLIPASE
SponsorABBVIE
Drug classVitamin C [EPC]
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about CREON

What is CREON?

CREON (LIPASE) is a Vitamin C [EPC] drug developed by ABBVIE.

Who makes CREON?

CREON is developed and marketed by ABBVIE (see full ABBVIE pipeline at /company/abbvie).

What is the generic name of CREON?

LIPASE is the generic (nonproprietary) name of CREON.

What drug class is CREON in?

CREON belongs to the Vitamin C [EPC] class. See all Vitamin C [EPC] drugs at /class/vitamin-c-epc.

What development phase is CREON in?

CREON is FDA-approved (marketed).

What are the side effects of CREON?

Common side effects of CREON include Headache, Contusion, Cough, Early Satiety, Abdominal Pain, Steatorrhea. Serious adverse events: Fibrosing Colonopathy, Distal Intestinal Obstruction Syndrome, Anaphylaxis, Asthma.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing