Lidocaine

Product NDC
68071-3792
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine
Dosage form
OINTMENT
Route
TOPICAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA086724
Marketing category
ANDA
Substance
LIDOCAINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3792-51 JAR in 1 CARTON (68071-3792-5) / 50 g in 1 JAR2025-02-13NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LIDOCAINE OINTMENT USP, 5% (Spearmint Flavored)NuCare Pharmaceuticals, Inc.2025-02-13HUMAN PRESCRIPTION DRUG LABEL1