Zenpep

Product NDC
0023-6115
11-digit product format
000236115
Labeler code
0023
Product ID
0023-6115_af3d1aff-3b2e-46a3-b114-9208dec8c67d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PANCRELIPASE LIPASE, PANCRELIPASE PROTEASE, PANCRELIPASE AMYLASE
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Allergan, Inc.
Application
BLA022210
Marketing category
BLA
Marketing start
2017-10-13
Marketing end
0000-00-00
Substance
PANCRELIPASE LIPASE; PANCRELIPASE PROTEASE; PANCRELIPASE AMYLASE
Active strength
5000 [USP'U]/1; [USP'U]/1; [USP'U]/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0023-6115-012023-01-31C16284748780-1f386c64a-3790-0266-e053-dadaa90a7c1af439e3a8-d60e-45f2-899c-d9be9b048b2d

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0023-6115-01EA - Each0023-611502ebe8cd-c028-46e0-9439-41ad465a2d9c12018-03-08

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0023-6115-0100023611501100 CAPSULE, DELAYED RELEASE in 1 BOTTLE, GLASS (0023-6115-01) 2017-10-130000-00-00NoNoCurrent