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Carnitor

CARNITOR (levocarnitine) Injection 1 g per 5 mL vial For Intravenous Use Only.

Approved
Approval ID

cf801cc4-775e-433d-9d32-e5d9a98981d3

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 20, 2023

Manufacturers
FDA

Leadiant Biosciences, Inc.

DUNS: 068301431

Products 1

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

levocarnitine

PRODUCT DETAILS

NDC Product Code54482-147
Application NumberNDA020182
Marketing CategoryC73594
Route of AdministrationINTRAVENOUS
Effective DateNovember 20, 2023
Generic Namelevocarnitine

INGREDIENTS (4)

HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
LEVOCARNITINEActive
Quantity: 1 g in 5 mL
Code: 0G389FZZ9M
Classification: ACTIB

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Carnitor - FDA Drug Approval Details