foscarbidopa 120 MG / foslevodopa 2400 MG per 10 ML Injection

RxCUI: 2695782
RxNorm name: foscarbidopa 120 MG / foslevodopa 2400 MG per 10 ML Injection
Display name: foscarbidopa 120 MG / foslevodopa 2400 MG per 10 ML Injection
Full name: foscarbidopa 120 MG / foslevodopa 2400 MG per 10 ML Injection
Term type: SY
Status: DailyMed mapping
Updated: 2026-06-04 23:38:51

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

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Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Vyalev	FOSCARBIDOPA/FOSLEVODOPA	AbbVie Inc.	28e806e4-951c-40a9-9f0c-d0929caf054c	2026-03-19	Warnings, Adverse reactions	Exact identifier rxcui: 2695782

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set ID	RxNorm string	TTY	SPL version	Label	Effective
28e806e4-951c-40a9-9f0c-d0929caf054c	foscarbidopa 120 MG / foslevodopa 2400 MG per 10 ML Injection	SY	6	These highlights do not include all the information needed to use VYALEV safely and effectively. See full prescribing information for VYALEV. VYALEV™ (foscarbidopa and foslevodopa) injection, for subcutaneous use Initial U.S. Approval: 1975	20260319
28e806e4-951c-40a9-9f0c-d0929caf054c	10 ML foscarbidopa 12 MG/ML / foslevodopa 240 MG/ML Injection	SCD	6	These highlights do not include all the information needed to use VYALEV safely and effectively. See full prescribing information for VYALEV. VYALEV™ (foscarbidopa and foslevodopa) injection, for subcutaneous use Initial U.S. Approval: 1975	20260319
28e806e4-951c-40a9-9f0c-d0929caf054c	foscarbidopa 120 MG / foslevodopa 2400 MG in 10 ML Injection	PSN	6	These highlights do not include all the information needed to use VYALEV safely and effectively. See full prescribing information for VYALEV. VYALEV™ (foscarbidopa and foslevodopa) injection, for subcutaneous use Initial U.S. Approval: 1975	20260319