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LIDOCAINE HCI

LIDOCAINE HCI JELLY, USP, 2%, 100mg URO-JET

Approved
Approval ID

95351883-ec37-f94a-e053-2995a90aa36a

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 25, 2024

Manufacturers
FDA

HF Acquisition Co LLC, DBA HealthFirst

DUNS: 045657305

Products 1

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

LIDOCAINE HCI

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code51662-1389
Application NumberANDA086283
Product Classification
M
Marketing Category
C73584
G
Generic Name
LIDOCAINE HCI
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 25, 2024
FDA Product Classification

INGREDIENTS (1)

LIDOCAINE HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: V13007Z41A
Classification: ACTIR

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LIDOCAINE HCI - FDA Drug Approval Details