Orange Book product · Brand (NDA)
DIAMOX
ACETAZOLAMIDE
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
ACETAZOLAMIDE
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
NDA 012945
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- —DIAMOXBrand (NDA)
NDA 008943 · TEVA BRANDED PHARM
- 2025ACETAZOLAMIDEGeneric (ANDA)
ANDA 212089 · AUROBINDO PHARMA LTD
- 2024ACETAZOLAMIDEGeneric (ANDA)
ANDA 218023 · EPIC PHARMA LLC
- 2024ACETAZOLAMIDEGeneric (ANDA)
ANDA 213706 · TORRENT
- 2023ACETAZOLAMIDEGeneric (ANDA)
ANDA 211151 · AJANTA PHARMA LTD
- 2023ACETAZOLAMIDEGeneric (ANDA)
ANDA 217197 · NE RX PHARMA
- 2023ACETAZOLAMIDEGeneric (ANDA)
ANDA 211069 · ZYDUS LIFESCIENCES
- 2021ACETAZOLAMIDEGeneric (ANDA)
ANDA 215101 · RUBICON RESEARCH
- 2021ACETAZOLAMIDEGeneric (ANDA)
ANDA 211372 · SOMERSET THERAPS LLC
- 2020ACETAZOLAMIDEGeneric (ANDA)
ANDA 214282 · MANKIND PHARMA
- 2020ACETAZOLAMIDEGeneric (ANDA)
ANDA 207401 · MICRO LABS LTD INDIA
- 2020ACETAZOLAMIDEGeneric (ANDA)
ANDA 207503 · BRECKENRIDGE
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
