lidocaine

Product NDC
71205-717
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lidocaine
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Proficient Rx LP
Application
ANDA206498
Marketing category
ANDA
Substance
LIDOCAINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-717-5050 g in 1 JAR (71205-717-50) 2022-11-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lidocaine Ointment, 5% for topical use DO NOT USE IN THE EYES Rx OnlyProficient Rx LP2022-11-01HUMAN PRESCRIPTION DRUG LABEL1