LIDOCAINE

Product NDC
80175-0418
11-digit product format
801750418
Labeler code
80175
Product ID
80175-0418_be2804cd-eb5f-d5e2-e053-2a95a90a4938
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LIDOCAINE
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Central Packaging
Application
ANDA206498
Marketing category
ANDA
Marketing start
2016-07-01
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
80175-0418-5LIDOCAINE50 g in 1 JAROINTMENT501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80175-0418LIDOCAINE OINTMENT [CENTRAL PACKAGING]1Legacy NDC, 1 package rows20210303_bc92d8aa-1524-6456-e053-2995a90a1cd3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1543069lidocaine 5 % Topical OintmentPSNbc92d8aa-1524-6456-e053-2995a90a1cd31
1543069lidocaine 0.05 MG/MG Topical OintmentSCDbc92d8aa-1524-6456-e053-2995a90a1cd31
1543069lidocaine 5 % Topical OintmentSYbc92d8aa-1524-6456-e053-2995a90a1cd31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80175-0418-58017504180550 g in 1 JAR (80175-0418-5) 50 g2016-07-010000-00-00NoNoCurrent