FDA.reportPublic FDA data

PRILOVIX Lite

Product NDC
72275-710
11-digit product format
722750710
Labeler code
72275
Product ID
72275-710_b8ce14ec-d886-1b6b-e053-2a95a90a0eb5
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
2019-03-17
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
72275-710-772025-03-10C16284748780-1f386c649-ae67-0266-e053-dadaa90a7c1a847d093f-a60d-9d7f-e053-2a91aa0ad547
72275-710-772023-01-30C16284748780-1f386c649-ae67-0266-e053-dadaa90a7c1a847d093f-a60d-9d7f-e053-2a91aa0ad547

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72275-710-77EA - Each72275-7101044f490-5e6c-46b2-bdcd-f20f8613c82912019-05-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72275-710-77722750710771 PACKAGE in 1 CARTON (72275-710-77) > 15 TUBE in 1 PACKAGE > 1 KIT in 1 TUBE * 30 g in 1 TUBE1 package2019-03-170000-00-00NoNoCurrent