FDA.reportPublic FDA data

PRILOVIX Ultralite Plus

Product NDC
72275-713
11-digit product format
722750713
Labeler code
72275
Product ID
72275-713_b8ce5529-4659-279c-e053-2995a90a43e2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lidocaine 2.5% and prilocaine 2.5%
Dosage form
KIT
Route
TOPICAL
Labeler
Primary Pharmaceuticals, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-07-08
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72275-713-772025-03-07C16284748780-1f386c649-eebb-0266-e053-dadaa90a7c1a8d428c85-367d-7154-e053-2995a90a716f
72275-713-772023-01-30C16284748780-1f386c649-eebb-0266-e053-dadaa90a7c1a8d428c85-367d-7154-e053-2995a90a716f

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72275-713-77EA - Each72275-71383603332-3196-45f2-beec-4ddc87ee516912019-11-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72275-713-77722750713771 PACKAGE in 1 CARTON (72275-713-77) > 10 TUBE in 1 PACKAGE > 1 KIT in 1 TUBE * 30 g in 1 TUBE1 package2019-07-080000-00-00NoNoCurrent