FDA.reportPublic FDA data

Aprizio Pak

Product NDC
59088-711
11-digit product format
590880711
Labeler code
59088
Product ID
59088-711_b4536ca8-6a1e-a6eb-e053-2995a90aabfc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lidocaine and prilocaine
Dosage form
KIT
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-06-06
Marketing end
0000-00-00
Active strength
0
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
59088-711-002024-02-21C16284748780-11030e365-5d9c-111a-e063-dadaa90a10e279b61785-669d-4016-a2a1-aedc20ab0ae9
59088-711-002024-01-30C16284748780-11030e365-5d9c-111a-e063-dadaa90a10e279b61785-669d-4016-a2a1-aedc20ab0ae9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59088-711-00EA - Each59088-7113ce9807b-47f7-46f4-adaf-6e1cfaaeb00312019-06-19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59088-711-00590880711001 KIT in 1 PACKAGE (59088-711-00) * 1 TUBE in 1 CARTON (0591-2070-30) > 30 g in 1 TUBE1 kit2018-06-060000-00-00NoNoCurrent