Home NDC 0378-2474 Diclofenac Potassium
Product NDC 0378-2474
11-digit product format 003782474
Labeler code 0378
Product ID 0378-2474_29742e42-c31f-497a-b8df-4efc6346c4e6
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name diclofenac potassium
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Mylan Pharmaceuticals Inc.
Application ANDA075463
Marketing category ANDA
Marketing start 1999-09-17
Marketing end 2024-02-29
Substance DICLOFENAC POTASSIUM
Active strength 50 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0378-2474-01 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0378-2474-01 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 0378-2474-01 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 0378-2474-01 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 0378-2474-01 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 0378-2474-01 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 0378-2474-01 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 0378-2474-01 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 0378-2474-01 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 0378-2474-01 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 0378-2474-01 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 0378-2474-01 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
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 A075463-001 DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB 1999-07-26
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A075463-001 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.
Product history page 1 of 2 · 42 observed 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 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB 1999-07-26 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB 1999-07-26 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB 1999-07-26 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB 1999-07-26 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 87673890dc5c…2021-03-12 10:30 UTC 2021-03 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 053a50430f4f…2023-01-26 05:58 UTC 2023-01 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A075463-001 DICLOFENAC POTASSIUM 50MG TABLET / ORAL AB RS 1999-07-26 e64feba35796…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 42 observed states.
DailyMed Product Concepts# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DICLOFENAC POTASSIUM ACTIVE INGREDIENT L4D5UA6CB4 DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 DICLOFENAC ACTIVE MOIETY 144O8QL0L1 DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 ANHYDROUS LACTOSE INACTIVE INGREDIENT 3SY5LH9PMK DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 DICLOFENAC POTASSIUM TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] 5
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 · 3 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Diclofenac Potassium DICLOFENAC POTASSIUM Marlex Pharmaceuticals, Inc. 30c7197b-7110-d8a7-e063-6394a90addfb 2025-03-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 075463 application number: ANDA075463 Diclofenac Potassium DICLOFENAC POTASSIUM Archis Pharma LLC 0d83cab3-c698-4763-9e77-27d72ba94e30 2024-12-30 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 075463 application number: ANDA075463 Diclofenac Potassium DICLOFENAC POTASSIUM NuCare Pharmaceuticals, Inc. 26a8f723-2a8e-8a5a-e063-6394a90a7bae 2024-11-11 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 075463 application number: ANDA075463
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0378-2474-01 00378247401 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2474-01) 1999-09-17 2024-02-29 No No Current