Home NDC 83831-142 KYXATA
Product NDC 83831-142
11-digit product format 838310142
Labeler code 83831
Product ID 83831-142_5c711945-70be-42f4-b153-e1459dd9929c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name CARBOplatin
Dosage form INJECTION
Route INTRAVENOUS
Labeler Avyxa Pharma, LLC
Application NDA219921
Marketing category NDA
Marketing start 2025-09-10
Substance CARBOPLATIN
Active strength 500 mg/50mL
Pharmacologic classes Platinum-based Drug [EPC], Platinum-containing Compounds [EXT]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
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 N219921-001 KYXATA CARBOPLATIN 20MG/2ML (10MG/ML) SOLUTION / INTRAVENOUS RLD 2025-08-08 N219921-002 KYXATA CARBOPLATIN 80MG/8ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 N219921-003 KYXATA CARBOPLATIN 500MG/50ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08
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 N219921-001 12427104 2045-04-01 Drug product 2025-10-02 N219921-002 12427104 2045-04-01 Drug product 2025-10-02 N219921-003 12427104 2045-04-01 Drug product 2025-10-02
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 2026-08-18 06:07:40 2026-07 N219921-001 KYXATA 20MG/2ML (10MG/ML) SOLUTION / INTRAVENOUS RLD 2025-08-08 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N219921-002 KYXATA 80MG/8ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N219921-003 KYXATA 500MG/50ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N219921-001 KYXATA 20MG/2ML (10MG/ML) SOLUTION / INTRAVENOUS RLD 2025-08-08 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N219921-002 KYXATA 80MG/8ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N219921-003 KYXATA 500MG/50ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N219921-001 KYXATA 20MG/2ML (10MG/ML) SOLUTION / INTRAVENOUS RLD 2025-08-08 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N219921-002 KYXATA 80MG/8ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N219921-003 KYXATA 500MG/50ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 31067a03dcf5…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N219921-001 KYXATA 20MG/2ML (10MG/ML) SOLUTION / INTRAVENOUS RLD 2025-08-08 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N219921-002 KYXATA 80MG/8ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N219921-003 KYXATA 500MG/50ML (10MG/ML) SOLUTION / INTRAVENOUS RLD, RS 2025-08-08 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 2026-08-18 06:07:40 2026-07 N219921-001 12427104 2045-04-01 Drug product 2025-10-02 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N219921-002 12427104 2045-04-01 Drug product 2025-10-02 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N219921-003 12427104 2045-04-01 Drug product 2025-10-02 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N219921-001 12427104 2045-04-01 Drug product 2025-10-02 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N219921-002 12427104 2045-04-01 Drug product 2025-10-02 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N219921-003 12427104 2045-04-01 Drug product 2025-10-02 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N219921-001 12427104 2045-04-01 Drug product 2025-10-02 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N219921-002 12427104 2045-04-01 Drug product 2025-10-02 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N219921-003 12427104 2045-04-01 Drug product 2025-10-02 31067a03dcf5…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N219921-001 12427104 2045-04-01 Drug product 2025-10-02 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N219921-002 12427104 2045-04-01 Drug product 2025-10-02 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N219921-003 12427104 2045-04-01 Drug product 2025-10-02 a50c72e98297…
Additional Listing Data#
Finished product Yes
Brand name base KYXATA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOPLATIN 500 mg/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BG3F62OND5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 597195 Internal RxNorm lookup 2721602 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 83831-142-50 KYXATA 1 in 1 CARTON INJECTION 1 6 83831-142-50 KYXATA 50 mL in 1 VIAL, MULTI-DOSE INJECTION 50 6
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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join KYXATA CARBOPLATIN Avyxa Pharma, LLC f91c48da-68d1-4aa7-89b8-d84a3e8b629b 2025-09-02 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (NDA): 219921 application number: NDA219921 ndc (product): 83831-142
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 83831-142-50 83831014250 1 VIAL, MULTI-DOSE in 1 CARTON (83831-142-50) / 50 mL in 1 VIAL, MULTI-DOSE 2025-09-10 No No Current