Lidocaine Hydrochloride

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 108250663

Effective Date

January 11, 2017

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Lidocaine(20 mg in 1 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

52584-015

Application Number

ANDA086283

Marketing Category

ANDA (C73584)

Route of Administration

TOPICAL

Effective Date

January 11, 2017

Ingredients

Code: V13007Z41AClass: ACTIRQuantity: 20 mg in 1 mL