Pancrelipase

Pancrelipase

Pancrelipase Recall

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Questions & Answers

Side Effects & Adverse Reactions

Should hypersensitivity occur, discontinue medication and treat symptomatically.

Legal Issues

There is currently no legal information available for this drug.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

Pancrelipase capsules are indicated for patients with exocrine pancreatic enzyme deficiency as in but not limited to: cystic fibrosis, chronic pancreatitis, post-pancreatectomy,  post-gastrointestinal bypass surgery (e.g. Billroth II gastroenterostomy), ductal obstruction from neoplasm (e.g. of the pancreas or common bile duct).

History

There is currently no drug history available for this drug.

Other Information

Pancrelipase 20,000 capsules are orally administered and contain delayed-release microspheres of porcine pancreatic enzyme concentrate, predominantly pancreatic lipase, amylase and protease.

Each 20,000 capsule contains:

Lipase 20,000 USP Units

Amylase 56,000 USP Units

Protease 44,000 USP Units

Inactive Ingredients:

Diethyl Phthalate NF, Hydroxypropyl Methylcellulose USP, Hypromellose Phthalate NF, Polyethylene Glycol NF, and Povidone USP.

Pancrelipase Manufacturers


  • Kaiser Foundation Hospitals
    Pancrelipase Capsule, Delayed Release [Kaiser Foundation Hospitals]
  • X-gen Pharmaceuticals, Inc.
    Pancrelipase Capsule, Delayed Release [X-gen Pharmaceuticals, Inc.]

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