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Lidocaine Hydrochloride

LidoRx (Lidocaine HCl USP) 3%

Approved
Approval ID

95ae61d8-d9a2-4e50-9065-c0cb97b95743

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 9, 2014

Manufacturers
FDA

Aidarex Pharmaceuticals LLC

DUNS: 801503249

Products 1

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

Lidocaine

PRODUCT DETAILS

NDC Product Code53217-064
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateJanuary 9, 2014
Generic NameLidocaine

INGREDIENTS (7)

LIDOCAINEActive
Quantity: 30 mg in 1 g
Code: 98PI200987
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)Inactive
Code: 809Y72KV36
Classification: IACT
ISOPROPYL ALCOHOLInactive
Code: ND2M416302
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
POLYSORBATE 20Inactive
Code: 7T1F30V5YH
Classification: IACT
TROLAMINEInactive
Code: 9O3K93S3TK
Classification: IACT

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Lidocaine Hydrochloride - FDA Drug Approval Details