LIDOCAINE

Product NDC
72189-165
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LIDOCAINE
Dosage form
OINTMENT
Route
TOPICAL
Labeler
DIRECT RX
Application
ANDA086724
Marketing category
ANDA
Substance
LIDOCAINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72189-165-3535.44 g in 1 BOTTLE (72189-165-35) 2021-01-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LIDOCAINEDIRECT RX2026-03-16HUMAN PRESCRIPTION DRUG LABEL7