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PANCRELIPASE - 0179-0020-70 - (PANCRELIPASE)

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Drug Information of PANCRELIPASE

Product NDC: 0179-0020
Proprietary Name: PANCRELIPASE
Non Proprietary Name: PANCRELIPASE
Active Ingredient(s): 56000; 20000; 44000    [USP'U]/1; [USP'U]/1; [USP'U]/1 & nbsp;   PANCRELIPASE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of PANCRELIPASE

Product NDC: 0179-0020
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100201

Package Information of PANCRELIPASE

Package NDC: 0179-0020-70
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOX, UNIT-DOSE (0179-0020-70)

NDC Information of PANCRELIPASE

NDC Code 0179-0020-70
Proprietary Name PANCRELIPASE
Package Description 30 CAPSULE, DELAYED RELEASE in 1 BOX, UNIT-DOSE (0179-0020-70)
Product NDC 0179-0020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PANCRELIPASE
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name PANCRELIPASE AMYLASE; PANCRELIPASE LIPASE; PANCRELIPASE PROTEASE
Strength Number 56000; 20000; 44000
Strength Unit [USP'U]/1; [USP'U]/1; [USP'U]/1
Pharmaceutical Classes

Complete Information of PANCRELIPASE


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