Home NDC 83831-149 VYKOURA
Product NDC 83831-149
11-digit product format 838310149
Labeler code 83831
Product ID 83831-149_c655613e-4381-461e-8e2d-4121be761c04
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name leucovorin calcium
Dosage form INJECTION
Route INTRAMUSCULAR; INTRAVENOUS
Labeler Avyxa Pharma, LLC
Application NDA220406
Marketing category NDA
Marketing start 2026-03-16
Substance LEUCOVORIN CALCIUM
Active strength 500 mg/50mL
Pharmacologic classes Folate Analog [EPC], Folic Acid [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N220406-001 VYKOURA LEUCOVORIN CALCIUM EQ 50MG BASE/5ML (EQ 10MG BASE/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS RLD, RS 2026-02-03 N220406-002 VYKOURA LEUCOVORIN CALCIUM EQ 350MG BASE/35ML (EQ 10MG BASE/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS RLD, RS 2026-02-03 N220406-003 VYKOURA LEUCOVORIN CALCIUM EQ 500MG BASE/50ML (EQ 10MG BASE/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS RLD, RS 2026-02-03
Orange Book patents# Current patent rows page 1 of 1 · 3 matching rows.
Application-product, Patent, Expiration table Application-product Patent Expiration Use code Coverage / status Submission date N220406-001 12564592 2044-12-23 Drug product 2026-03-05 N220406-002 12564592 2044-12-23 Drug product 2026-03-05 N220406-003 12564592 2044-12-23 Drug product 2026-03-05
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N220406-001 VYKOURA EQ 50MG BASE/5ML (EQ 10MG BASE/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS RLD, RS 2026-02-03 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N220406-002 VYKOURA EQ 350MG BASE/35ML (EQ 10MG BASE/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS RLD, RS 2026-02-03 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N220406-003 VYKOURA EQ 500MG BASE/50ML (EQ 10MG BASE/ML) SOLUTION / INTRAMUSCULAR, INTRAVENOUS RLD, RS 2026-02-03 a50c72e98297…
Observed Orange Book patent history# Captured, Edition, Application-product table Captured Edition Application-product Patent Expiration Use code Coverage / status Submission date Source SHA-256 2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N220406-001 12564592 2044-12-23 Drug product 2026-03-05 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N220406-002 12564592 2044-12-23 Drug product 2026-03-05 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N220406-003 12564592 2044-12-23 Drug product 2026-03-05 a50c72e98297…
Additional Listing Data#
Finished product Yes
Brand name base VYKOURA
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LEUCOVORIN CALCIUM 500 mg/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RPR1R4C0P4 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 6 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2104714 Internal RxNorm lookup 2735355 Internal RxNorm lookup 2735359 Internal RxNorm lookup 2735364 Internal RxNorm lookup 2735365 Internal RxNorm lookup 2735366 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83831-149-50 VYKOURA 50 mL in 1 VIAL, SINGLE-USE INJECTION 50 7 83831-149-50 VYKOURA 1 in 1 CARTON INJECTION 1 7
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.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 83831-149-50 83831014950 1 VIAL, SINGLE-USE in 1 CARTON (83831-149-50) / 50 mL in 1 VIAL, SINGLE-USE 2026-03-16 No No Current