Lidocaine Hydrochloride
Lidocaine HydrochlorideInjection, USP
Approved
Approval ID
22ebe9b5-91d9-43eb-a52c-1523def30159
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 28, 2014
Manufacturers
FDA
US MedSource, LLC
DUNS: 032793851
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
LIDOCAINE HYDROCHLORIDE ANHYDROUS
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code61699-4276
Application NumberANDA088299
Product Classification
M
Marketing Category
C73584
G
Generic Name
LIDOCAINE HYDROCHLORIDE ANHYDROUS
Product Specifications
Route of AdministrationINFILTRATION
Effective DateJune 3, 2014
FDA Product Classification
INGREDIENTS (6)
LIDOCAINE HYDROCHLORIDEActive
Quantity: 10 mg in 1 mL
Code: V13007Z41A
Classification: ACTIR
SODIUM CHLORIDEInactive
Quantity: 7 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
METHYLPARABENInactive
Quantity: 1 mg in 1 mL
Code: A2I8C7HI9T
Classification: IACT