Lidocaine

Product NDC
0143-9577
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine Hydrochloride
Dosage form
INJECTION, SOLUTION
Route
INFILTRATION; PERINEURAL
Labeler
Hikma Pharmaceuticals USA Inc.
Application
ANDA080407
Marketing category
ANDA
Substance
LIDOCAINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0143-9577-1010 VIAL, MULTI-DOSE in 1 PACKAGE (0143-9577-10) / 50 mL in 1 VIAL, MULTI-DOSE (0143-9577-01) 1972-02-14NoHistorical

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