lidocaine

Product NDC
80175-0008
11-digit product format
801750008
Labeler code
80175
Product ID
80175-0008_bd995ea8-a074-5cac-e053-2995a90a3ddd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lidocaine
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Central Packaging
Application
ANDA205318
Marketing category
ANDA
Marketing start
2017-02-27
Marketing end
0000-00-00
Substance
LIDOCAINE
Active strength
50 mg/g
Pharmacologic classes
Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80175-0008-5lidocaine50 g in 1 JAROINTMENT501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80175-0008LIDOCAINE OINTMENT [CENTRAL PACKAGING]1Legacy NDC, 1 package rows20210225_bc028dba-b823-0eeb-e053-2a95a90a7905.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1543069lidocaine 5 % Topical OintmentPSNbc028dba-b823-0eeb-e053-2a95a90a79051
1543069lidocaine 0.05 MG/MG Topical OintmentSCDbc028dba-b823-0eeb-e053-2a95a90a79051
1543069lidocaine 5 % Topical OintmentSYbc028dba-b823-0eeb-e053-2a95a90a79051

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80175-0008-58017500080550 g in 1 JAR (80175-0008-5) 50 g2017-02-270000-00-00NoNoCurrent