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Levorphanol Tartrate

LEVORPHANOL TARTRATE TABLETS USP, CII

Approved
Approval ID

6e7ca993-c8b9-4510-a2b0-5bcc678d2571

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 25, 2020

Manufacturers
FDA

Virtus Pharmaceuticals, LLC

DUNS: 079659493

Products 1

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

Levorphanol Tartrate

PRODUCT DETAILS

NDC Product Code69543-417
Application NumberANDA211484
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateSeptember 1, 2020
Generic NameLevorphanol Tartrate

INGREDIENTS (4)

LEVORPHANOL TARTRATEActive
Quantity: 2 mg in 1 1
Code: 04WQU6T9QI
Classification: ACTIB
ANHYDROUS LACTOSEInactive
Code: 3SY5LH9PMK
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
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Levorphanol Tartrate - FDA Approval | MedPath