Home NDC 33342-340 Fenofibrate
Product NDC 33342-340
11-digit product format 333420340
Labeler code 33342
Product ID 33342-340_ab7aad70-2879-4260-831e-cbfbe8be73b2
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Fenofibrate
Dosage form TABLET
Route ORAL
Labeler Macleods Pharmaceuticals Limited
Application ANDA210248
Marketing category ANDA
Marketing start 2024-11-13
Substance FENOFIBRATE
Active strength 145 mg/1
Pharmacologic classes Peroxisome Proliferator Receptor alpha Agonist [EPC]
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 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A210248-001 FENOFIBRATE FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 A210248-002 FENOFIBRATE FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
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 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 2680178bc6a6…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A210248-001 FENOFIBRATE 48MG TABLET / ORAL AB 2024-11-13 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A210248-002 FENOFIBRATE 145MG TABLET / ORAL AB 2024-11-13 a50c72e98297…
Observed Orange Book normalized TE history# Additional Listing Data#
Finished product Yes
Brand name base Fenofibrate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FENOFIBRATE 145 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U202363UOS Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 477560 Internal RxNorm lookup 477562 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 33342-340-07 Fenofibrate 30 in 1 BOTTLE TABLET 30 2 33342-340-10 Fenofibrate 90 in 1 BOTTLE TABLET 90 2 33342-340-12 Fenofibrate 10 in 1 BLISTER PACK TABLET 10 2 33342-340-12 Fenofibrate 10 in 1 CARTON TABLET 10 2 33342-340-15 Fenofibrate 500 in 1 BOTTLE TABLET 500 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 33342-340 FENOFIBRATE TABLET [MACLEODS PHARMACEUTICALS LIMITED] 1 Current NDC, 5 package rows 20250210_e8b9d1f5-0541-424f-b1d4-bef6381aa934.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 · 1 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 33342-340-07 33342034007 30 TABLET in 1 BOTTLE (33342-340-07) 30 tablet 2024-11-13 No No Current 33342-340-10 33342034010 90 TABLET in 1 BOTTLE (33342-340-10) 90 tablet 2024-11-13 No No Current 33342-340-12 33342034012 10 BLISTER PACK in 1 CARTON (33342-340-12) / 10 TABLET in 1 BLISTER PACK 10 blister pack 2024-11-13 No No Current 33342-340-15 33342034015 500 TABLET in 1 BOTTLE (33342-340-15) 500 tablet 2024-11-13 No No Current