Application 018922

Type
NDA
Sponsor
WYETH PHARMS INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
002LODINEETODOLACCAPSULE;ORAL200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
003LODINEETODOLACCAPSULE;ORAL300MGYesNo
004LODINEETODOLACTABLET;ORAL400MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
005LODINEETODOLACTABLET;ORAL500MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N018922-002LODINEETODOLAC200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-31
N018922-003LODINEETODOLAC300MGCAPSULE / ORALRLD1991-01-31
N018922-004LODINEETODOLAC400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-29
N018922-005LODINEETODOLAC500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-28

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 5 · 172 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-3184e616aacf4f…
2026-09-14 22:38:342026-08N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-3184e616aacf4f…
2026-09-14 22:38:342026-08N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-2984e616aacf4f…
2026-09-14 22:38:342026-08N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-2884e616aacf4f…
2026-08-18 06:07:402026-07N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-31caaa826d4ba7…
2026-08-18 06:07:402026-07N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-31caaa826d4ba7…
2026-08-18 06:07:402026-07N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-29caaa826d4ba7…
2026-08-18 06:07:402026-07N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-28caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-31011fe1cb6892…
2026-02-19 14:30 UTC2026-02N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-31011fe1cb6892…
2026-02-19 14:30 UTC2026-02N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-29011fe1cb6892…
2026-02-19 14:30 UTC2026-02N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-28011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-3131067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-3131067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-2931067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-2831067a03dcf5…
2025-08-23 18:47 UTC2025-08N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-316a471c1ec25d…
2025-08-23 18:47 UTC2025-08N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-316a471c1ec25d…
2025-08-23 18:47 UTC2025-08N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-296a471c1ec25d…
2025-08-23 18:47 UTC2025-08N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-286a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-31fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-31fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-29fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-28fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-31b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-31b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-29b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-28b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-3103ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-3103ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-2903ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-2803ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-312680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-312680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-292680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-282680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N018922-002LODINE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1991-01-315bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N018922-003LODINE300MGCAPSULE / ORALRLD1991-01-315bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N018922-004LODINE400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1993-07-295bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N018922-005LODINE500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1996-06-285bbf6a4d5a75…

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 2 of 4 · 73 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
etodolacETODOLACIpca Laboratories Limitedf50a93ca-584a-4205-a79b-31bafdd309c22026-01-29Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
etodolacETODOLACIpca Laboratories Limitedd583988c-3e7e-4415-b2fd-34049791cd1c2026-01-21Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACA-S Medication Solutions336d5331-4d60-42e2-8cfc-aad57c01eda02026-01-13Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACA-S Medication Solutions00125d63-d8d0-46c5-bdf1-80d2c85eda5a2026-01-13Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACA-S Medication Solutions4d392c1b-95c2-4925-98bf-0203c412d3da2026-01-05Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACNorthwind Health Company, LLC7ec87ffd-057e-420c-b8f2-0a6eed4152be2026-01-01Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACNorthwind Health Company, LLCb0880f39-a6fa-23ab-e053-2995a90a7eb22026-01-01Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACNorthwind Health Company, LLCda34581d-3066-711c-e053-2995a90a8e842026-01-01Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACANI Pharmaceuticals, Inc.420c7b62-3bea-4d6b-82e0-ab1c176c7f1e2025-12-22Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACEdenbridge Pharmaceuticals LLC.bf1afcd5-e1da-4874-981f-f252cb0b32c22025-12-17Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACPD-Rx Pharmaceuticals, Inc.80e9d756-9278-48bb-bfdd-7d070ae0f3412025-12-16Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACChartwell RX, LLCf86d2b22-d3f7-49cd-98f6-cdb2bd8551922025-12-09Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACUnichem Pharmaceuticals (USA), Inc.18215cb7-c833-4a98-a61d-4bedf518a3802025-12-09Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACBryant Ranch Prepack479bce92-2066-46ed-b4bb-8c7a59edfffd2025-11-14Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACBryant Ranch Prepack5e94a98f-d36e-4f28-b79c-6ad8a67933812025-10-22Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACApotex Corp.4d682f98-1e8a-4c2b-6df3-169d2ed10dc12025-09-18Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACAdvanced Rx of Tennessee, LLC3d865ff0-fc45-1e95-e063-6294a90a8e182025-08-29Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACNORTHSTAR RX LLC107ea9d7-80a9-41a4-b61e-1683701273192025-06-24Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACPreferred Pharmaceuticals Inc.556a7d5f-2c3c-4efb-ac0c-fca1407916022025-03-24Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC
EtodolacETODOLACA-S Medication Solutionsa7d91fcf-7928-4c9e-862b-6922d6e47c9d2025-02-06Boxed warning, Warnings, Adverse reactionsName fallback
generic name: ETODOLAC

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
57655SUPPL2019-02-15
33648SUPPL2015-07-27
16096SUPPL2007-10-15
33647SUPPL2006-01-20
16095SUPPL2006-01-20
16094SUPPL2005-05-27
11362SUPPL2005-05-27