Home NDC 72603-261 Rufinamide
Product NDC 72603-261
11-digit product format 726030261
Labeler code 72603
Product ID 72603-261_1ccfda8b-0fa1-6b4a-e063-6294a90a15ad
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Rufinamide
Dosage form SUSPENSION
Route ORAL
Labeler NorthStar RxLLC
Application ANDA216841
Marketing category ANDA
Marketing start 2024-08-01
Substance RUFINAMIDE
Active strength 40 mg/mL
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 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A216841-001 RUFINAMIDE RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A216841-001 AB
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 2026-02-19 14:30 UTC 2026-02 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 8072bd15b7f6…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 ea1830bbd6c7…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A216841-001 RUFINAMIDE 40MG/ML SUSPENSION / ORAL AB 2023-12-05 a50c72e98297…
Observed Orange Book normalized TE history# Additional Listing Data#
Finished product Yes
Brand name base Rufinamide
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RUFINAMIDE 40 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WFW942PR79 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1092357 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 72603-261-01 Rufinamide 1 in 1 CARTON SUSPENSION 1 1 72603-261-01 Rufinamide 460 mL in 1 BOTTLE SUSPENSION 460 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72603-261 RUFINAMIDE (RUFINAMIDE) SUSPENSION [NORTHSTAR RXLLC] 1 Current NDC, 2 package rows 20240802_b682021c-74c3-4cc8-84af-acd94438397a.zip
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 · 2 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72603-261-01 72603026101 1 BOTTLE in 1 CARTON (72603-261-01) / 460 mL in 1 BOTTLE 1 bottle 2024-08-01 No No Current