Home NDC 0113-0604-93 good sense ibuprofen
Product NDC 0113-0604
Requested package NDC 0113-0604-93
11-digit product format 001130604
Labeler code 0113
Product ID 0113-0604_822f5bcb-7dcf-454a-8d76-8ce8aaa40d4c
Type HUMAN OTC DRUG
Nonproprietary name Ibuprofen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler L. Perrigo Company
Application ANDA072096
Marketing category ANDA
Marketing start 1989-09-15
Substance IBUPROFEN
Active strength 200 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 A072096-001 IBUPROFEN IBUPROFEN 200MG TABLET / ORAL 1987-12-08
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 · 41 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 2026-02-19 14:30 UTC 2026-02 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 87673890dc5c…2021-03-12 10:30 UTC 2021-03 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 053a50430f4f…2023-01-26 05:58 UTC 2023-01 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A072096-001 IBUPROFEN 200MG TABLET / ORAL 1987-12-08 cb3db0bc1861…
Additional Listing Data#
Finished product Yes
Brand name base good sense ibuprofen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IBUPROFEN 200 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WK2XYI10QM Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 310965 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 0113-0604-02 good sense ibuprofen 550 in 1 BOTTLE TABLET, FILM COATED 550 11 0113-0604-52 good sense ibuprofen 10 in 1 VIAL TABLET, FILM COATED 10 11 0113-0604-62 good sense ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 11 0113-0604-62 good sense ibuprofen 24 in 1 BOTTLE TABLET, FILM COATED 24 11 0113-0604-71 good sense ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 11 0113-0604-71 good sense ibuprofen 50 in 1 BOTTLE TABLET, FILM COATED 50 11 0113-0604-76 good sense ibuprofen 120 in 1 BOTTLE TABLET, FILM COATED 120 11 0113-0604-76 good sense ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 11 0113-0604-78 good sense ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 11 0113-0604-78 good sense ibuprofen 100 in 1 BOTTLE TABLET, FILM COATED 100 11 0113-0604-82 good sense ibuprofen 100 in 1 BOTTLE TABLET, FILM COATED 100 11 0113-0604-82 good sense ibuprofen 2 in 1 CARTON TABLET, FILM COATED 2 11 0113-0604-85 good sense ibuprofen 250 in 1 BOTTLE TABLET, FILM COATED 250 11 0113-0604-90 good sense ibuprofen 500 in 1 BOTTLE TABLET, FILM COATED 500 11 0113-0604-93 good sense ibuprofen 1000 in 1 BOTTLE TABLET, FILM COATED 1000 11
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded IBUPROFEN ACTIVE INGREDIENT WK2XYI10QM GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 IBUPROFEN ACTIVE MOIETY WK2XYI10QM GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 FERRIC OXIDE RED INACTIVE INGREDIENT 1K09F3G675 GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 FERRIC OXIDE YELLOW INACTIVE INGREDIENT EX438O2MRT GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0113-0604 GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L. PERRIGO COMPANY] 10 Current NDC, Legacy NDC, 15 package rows 20250418_70d0a429-27c1-43a5-b2ea-a9919e0910f8.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 4 · 67 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join IBUPROFEN IBUPROFEN Amazon.com Services LLC b5a47efe-222f-4cbd-b649-caafd16a0829 2026-07-29 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN HyVee Inc e7175dc9-db39-4452-a419-85af179de422 2026-07-16 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 good sense ibuprofen IBUPROFEN Bryant Ranch Prepack d6460cc3-c207-44e0-bf78-ad6fef055ed5 2026-07-09 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN Unit Dose Solutions, Inc. 551535ce-eab0-bb13-e063-6294a90a2070 2026-06-25 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 Berkley and Jensen Ibuprofen IBUPROFEN BJWC cda57e42-6106-46ee-82d1-479a692ee5bb 2026-05-21 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 good neighbor pharmacy ibuprofen IBUPROFEN Amerisource Bergen 085dcc1a-e4b0-4d08-9476-72275382d1a1 2026-05-15 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 good sense ibuprofen IBUPROFEN Preferred Pharmaceuticals Inc. f1a03b1f-2d87-43cc-b256-bd296ccd09f2 2026-05-13 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN Kroger Company 6307485a-8be6-40ee-899b-00eb3ee8ce61 2026-05-01 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 CounterAct IB IBUPROFEN Melaleuca, Inc 7fafc13e-3fee-ace3-e053-2a91aa0ac2ea 2026-03-17 Boxed warning, Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 Leader Ibuprofen IBUPROFEN Cardinal Health 110, LLC. dba Leader d673266c-3d2b-479f-9b53-cdd1b8651393 2026-02-25 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN HyVee Inc 4c24c884-55f7-40b4-8d6f-db6144d5ebcb 2026-02-05 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN HyVee Inc 5233c409-3743-4312-9f75-14ded6755b5c 2026-02-02 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 equate ibuprofen IBUPROFEN Wal-Mart Stores Inc b29034a6-657b-426f-a41a-5e64c4bc759d 2026-01-20 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN CVS Pharmacy ace493e6-91bc-41aa-8e5c-5bc14981de91 2026-01-06 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN Northwind Health Company, LLC da6c2802-5d15-dbcb-e053-2a95a90a2561 2026-01-01 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 good sense ibuprofen IBUPROFEN L. Perrigo Company 70d0a429-27c1-43a5-b2ea-a9919e0910f8 2025-12-22 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ndc (package): 0113-0604-93 ndc (product): 0113-0604 ndc11 (package): 00113060493 ibuprofen IBUPROFEN NuCare Pharmaceuticals, Inc. 463ea713-6b27-b00b-e063-6394a90a8646 2025-12-18 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 ibuprofen IBUPROFEN PD-Rx Pharmaceuticals, Inc. 96bff700-bca3-4b94-b8a2-379102721db8 2025-12-15 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 good sense ibuprofen IBUPROFEN Preferred Pharmaceuticals Inc. c447fc6b-e9ef-447a-9609-5f893e18dfa7 2025-11-17 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096 GOODNOW PAIN RELIEF IBUPROFEN Gobrands, Inc 0759085d-6ac3-446b-ac2c-8dc30e32e1d1 2025-11-08 Warnings Exact identifier application applno (ANDA): 072096 application number: ANDA072096
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 0113-0604-93 00113060493 1000 TABLET, FILM COATED in 1 BOTTLE (0113-0604-93) 2007-05-31 0000-00-00 No No Current