Application 008943

Type
NDA
Sponsor
TEVA BRANDED PHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DIAMOXACETAZOLAMIDETABLET;ORAL125MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
002DIAMOXACETAZOLAMIDETABLET;ORAL250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo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 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N008943-001DIAMOXACETAZOLAMIDE125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982
N008943-002DIAMOXACETAZOLAMIDE250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982

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 3 · 86 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198284e616aacf4f…
2026-08-18 06:07:402026-07N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198231067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198231067a03dcf5…
2025-08-23 18:47 UTC2025-08N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19826a471c1ec25d…
2025-08-23 18:47 UTC2025-08N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19826a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198203ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198203ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19822680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19822680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19825bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19825bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982d8e5a09893c0…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982d06236e962d9…
2024-10-29 15:01 UTC2024-10N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198279d66fd596c7…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 198279d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982301d65b070ca…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 1982301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19821e350fbaab3a…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19821e350fbaab3a…
2024-05-31 18:47 UTC2024-05N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19828072bd15b7f6…
2024-05-31 18:47 UTC2024-05N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19828072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19825c6f7cd8ea54…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD, Approved before 19825c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N008943-001DIAMOX125MGTABLET / ORALRLD, Approved before 19825d02ea3f76ae…
2022-04-08 23:34 UTC2022-04N008943-002DIAMOX250MGTABLET / ORALRLD, Approved before 19825d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N008943-001DIAMOX125MGTABLET / ORALRLD, Approved before 19824b0b4de00fa7…
2022-04-04 05:41 UTC2022-04N008943-002DIAMOX250MGTABLET / ORALRLD, Approved before 19824b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N008943-001DIAMOX125MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**TABLET / ORALRLD, Approved before 198274a2ff9319b5…
2019-12-13 00:20 UTC2019-12N008943-002DIAMOX250MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**TABLET / ORALRLD, Approved before 198274a2ff9319b5…

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 3 · 51 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetazolamideACETAZOLAMIDEStrides Pharma Science Limited4813b9dd-5f58-44bb-ad64-cdb3318280802026-08-19Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEPD-Rx Pharmaceuticals, Inc.268db224-d5db-457c-86bc-972c9fe079172026-07-07Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
acetazolamideACETAZOLAMIDEMajor Pharmaceuticals37135ba5-63fd-427f-9b4a-8b7d1009bbca2026-05-28Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEA-S Medication Solutionsc5acf531-ba55-47b7-88db-e5da0206ebf12026-05-22Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEBryant Ranch Prepack71f1fbbb-428e-4bf7-bc20-2946c1079bd32026-05-20Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
acetazolamideACETAZOLAMIDEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.0700a910-79aa-4431-aecf-637fe14fcae82026-05-12Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
acetazolamideACETAZOLAMIDEA-S Medication Solutions07fd0bde-8f7c-47d2-9e81-2c1eee259fa62026-05-01Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEREMEDYREPACK INC.fb2cf8fe-da81-445e-a18b-9aa9ced1d34a2026-04-28Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.4dd56001-4941-4ff0-9f30-02a1bcc4fe7e2026-04-10Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
acetazolamideACETAZOLAMIDEBryant Ranch Prepack0d903375-c583-4362-9f8a-f7b74ce01e0b2026-04-09Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEBryant Ranch Prepack9af15152-d46f-4bc3-a16e-b70a472bc52a2026-03-23Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEBryant Ranch Prepack84a582a9-c7e5-4159-a5eb-a47a96b4afc02026-03-23Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEBryant Ranch Prepackf7227cc5-0a80-47df-baf8-09f1b22b187e2026-03-20Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDELifestar Pharma LLC0913db35-3f08-4d82-8394-486bd9a487c42026-03-17Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.33d912ea-9e1c-49eb-bd93-f0b1b2da67b62026-02-26Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
acetazolamideACETAZOLAMIDEAvKAREd6fba129-ac6e-4d04-bd09-8470be4e7ecc2026-02-24Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEWestminster Pharmaceuticals, LLC417b1df2-63bc-473c-9e02-5f93dd45554d2026-02-17Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
acetaZOLAMIDEACETAZOLAMIDEA-S Medication Solutionsb339843f-0324-4996-88a0-0619fd6f867b2026-02-13Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEMarlex Pharmaceuticals, Inc.4a03f35d-bfcb-77ff-e063-6294a90a4f062026-02-01Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE
AcetazolamideACETAZOLAMIDEANI Pharmaceuticals, Inc.bde94a48-05d0-45a0-a589-ec05b7d165322026-01-23Warnings, Adverse reactionsName fallback
generic name: ACETAZOLAMIDE

Reported adverse events (FAERS/openFDA)#

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

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
83641SUPPL 2025-10-03
83633SUPPL 2025-10-02
79710SUPPL 2024-09-24
79694SUPPL 2024-09-23
71085SUPPL2022-05-17
71080SUPPL2022-05-16