01 1Avet Pharmaceuticals
02 1ENDO OPERATIONS
03 1Ebb Medical AB
04 1Hikma Pharmaceuticals
05 1Hospira, Inc.
06 1MARCAN PHARMACEUTICALS INC
07 1Mercury Pharmaceuticals Ltd,
08 1ORIFARM GROUP AS
09 1Paranova Group AS
10 1Quad Pharma
11 1STERIMAX INC
12 1Teva Pharmaceutical Industries
13 1Viatris
14 1XGen Pharmaceuticals
15 1Zydus Pharmaceuticals
01 8INJECTABLE;INJECTION
02 1Injectable; Injection
03 2POWDER FOR SOLUTION
04 4POWDER FOR SOLUTION FOR INJECTION
01 3DISCN
02 2Prescription
03 5RX
04 5Blank
01 1ACETAZOLAMIDE FOR INJECTION USP
02 1ACETAZOLAMIDE FOR INJECTION, USP
03 8ACETAZOLAMIDE SODIUM
04 1DIAMOX
05 4Diamox
01 2Canada
02 4Sweden
03 9USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2014-12-19
Application Number : 202693
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1995-02-28
Application Number : 40089
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1995-10-30
Application Number : 40108
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
ACETAZOLAMIDE (ACETAZOLAMIDE SODIUM)
Brand Name : ACETAZOLAMIDE FOR INJECTION USP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date :
Application Number : 2537893
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info :
Registration Country : Sweden
Brand Name : Diamox
Dosage Form : POWDER FOR SOLUTION FOR INJECTION
Dosage Strength : 500 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Diamox
Dosage Form : POWDER FOR SOLUTION FOR INJECTION
Dosage Strength : 500 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : Injectable; Injection
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date :
Application Number : 89619
Regulatory Info :
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
ACETAZOLAMIDE (ACETAZOLAMIDE SODIUM)
Brand Name : ACETAZOLAMIDE FOR INJECTION, USP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date :
Application Number : 2358328
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DIAMOX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 9388
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2012-05-09
Application Number : 200880
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2008-12-10
Application Number : 40784
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2019-04-15
Application Number : 206533
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ACETAZOLAMIDE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2017-06-20
Application Number : 205358
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Sweden
Brand Name : Diamox
Dosage Form : POWDER FOR SOLUTION FOR INJECTION
Dosage Strength : 500 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Sweden
Brand Name : Diamox
Dosage Form : POWDER FOR SOLUTION FOR INJECTION
Dosage Strength : 500 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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