United States · FDA National Drug Code directory

Vyalev

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0074-0501_1f0fe652-c027-4b61-9ba4-78548dd48e89
Product NDC
0074-0501
Form
INJECTION
Composition / generic term
foscarbidopa/foslevodopa
Labeler
AbbVie Inc.
Marketing category
NDA
Marketing start / end (source format)
20220412
Source listing expiry
20271231

Source-listed ingredients

  • FOSCARBIDOPA — 12 mg/mL
  • FOSLEVODOPA — 240 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 7 VIAL, SINGLE-DOSE in 1 CARTON (0074-0501-01) / 10 mL in 1 VIAL, SINGLE-DOSE · 0074-0501-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →