LIDOCAINE HYDROCHLORIDE

Product NDC
51662-1552
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LIDOCAINE HYDROCHLORIDE
Dosage form
JELLY
Route
TOPICAL
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Application
ANDA086283
Marketing category
ANDA
Substance
LIDOCAINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
51662-1552-325 POUCH in 1 CASE (51662-1552-3) / 1 CARTON in 1 POUCH (51662-1552-2) / 1 VIAL, SINGLE-USE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-USE2021-06-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LIDOCAINE HYDROCHLORIDE JELLY USP, 2% 200mg (20mg/mL) 10mL URO-JET®HF Acquisition Co LLC, DBA HealthFirst2024-01-30HUMAN PRESCRIPTION DRUG LABEL2