Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2Aspen API

02 1ABRAXIS PHARM

03 1ANI Pharmaceuticals Inc

04 7Actavis Inc

05 1Akrikhin

06 2Amneal Pharmaceuticals

07 6Aurobindo Pharma Limited

08 2Avet Pharmaceuticals

09 1BEDFORD LABS

10 1Celogen Pharma Pvt. Ltd

11 3Chartwell Pharmaceuticals llc

12 4Fosun Pharmaceutical

13 1GSK

14 2Glenmark Pharmaceuticals

15 3Gulf Drug Company

16 2HEATHER

17 3Hikma Pharmaceuticals

18 3Holden Medical Laboratories Pvt. Ltd

19 1Hospira, Inc.

20 4Infugen Pharma

21 2Interpharm

22 1Keko Pharmaceutical Industries

23 1Lupin Ltd

24 2MARTEC USA LLC

25 1Macure Pharma

26 1Madras Pharmaceuticals

27 2Mutual Pharmaceutical Company, Inc.

28 1NASKA

29 1NoroBio Pharmaceutical

30 2Novel Laboratories, Inc.

31 1Novitium Pharma LLC

32 2PHARM ASSOC

33 5Pfizer Inc

34 2Pliva Hrvatska

35 1Pluviaendo

36 1Prasco Laboratories

37 1Quad Pharma

38 2ROXANE

39 2SUPERPHARM

40 2Shionogi

41 1Somerset Pharmaceuticals Inc

42 2Stivaph Healthcare

43 7Sun Pharmaceutical Industries Limited

44 7Teva Pharmaceutical Industries

45 4USL PHARMA

46 3Vaishali Pharma Ltd

47 1Viatris

48 3Vista Pharmaceuticals

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API.

Regulatory Info :

Registration Country : Sweden

Flera substanser, se innehåll

Brand Name : Eusaprim

Dosage Form : ORAL SUSPENSION

Dosage Strength : 8 MG/ML+40 MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Aspen API Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API.

Regulatory Info :

Registration Country : Sweden

Flera substanser, se innehåll

Brand Name : Eusaprim

Dosage Form : KONCENTRAT TILL INFUSIONSVÄTSKA, LÖSNING

Dosage Strength : 16 MG/ML+80 MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Aspen API Comapny Banner

03

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1983-05-09

Application Number : 18852

Regulatory Info : DISCN

Registration Country : USA

blank

04

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM DOUBLE STRENGTH

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1983-05-09

Application Number : 18854

Regulatory Info : DISCN

Registration Country : USA

blank

05

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1984-11-07

Application Number : 70000

Regulatory Info : DISCN

Registration Country : USA

blank

06

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1984-11-07

Application Number : 70002

Regulatory Info : DISCN

Registration Country : USA

blank

07

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML

Packaging :

Approval Date : 1987-06-02

Application Number : 70028

Regulatory Info : DISCN

Registration Country : USA

blank

08

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1982-05-19

Application Number : 18598

Regulatory Info : DISCN

Registration Country : USA

blank

09

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM DOUBLE STRENGTH

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1982-05-19

Application Number : 18598

Regulatory Info : DISCN

Registration Country : USA

blank

10

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1984-11-14

Application Number : 70006

Regulatory Info : DISCN

Registration Country : USA

blank

11

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM DOUBLE STRENGTH

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1984-11-14

Application Number : 70007

Regulatory Info : DISCN

Registration Country : USA

blank

12

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1985-02-15

Application Number : 70022

Regulatory Info : DISCN

Registration Country : USA

blank

13

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SEPTRA

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1982-01-01

Application Number : 17376

Regulatory Info : RX

Registration Country : USA

blank

14

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SEPTRA DS

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1982-01-01

Application Number : 17376

Regulatory Info : RX

Registration Country : USA

blank

15

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SEPTRA

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 17598

Regulatory Info : DISCN

Registration Country : USA

blank

16

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SEPTRA GRAPE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1986-02-12

Application Number : 17598

Regulatory Info : DISCN

Registration Country : USA

blank

17

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SEPTRA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 80MG/ML;16MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 18452

Regulatory Info : DISCN

Registration Country : USA

blank

18

PHARM ASSOC

U.S.A
Fi Europe 2024
Not Confirmed
arrow

PHARM ASSOC

U.S.A
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFATRIM PEDIATRIC

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML

Packaging :

Approval Date : 1983-01-07

Application Number : 18615

Regulatory Info : RX

Registration Country : USA

blank

19

PHARM ASSOC

U.S.A
Fi Europe 2024
Not Confirmed
arrow

PHARM ASSOC

U.S.A
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFATRIM

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML

Packaging :

Approval Date : 1983-01-07

Application Number : 18615

Regulatory Info : DISCN

Registration Country : USA

blank

20

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : BACTRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1982-01-01

Application Number : 17377

Regulatory Info : RX

Registration Country : USA

blank

21

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : BACTRIM DS

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1982-01-01

Application Number : 17377

Regulatory Info : RX

Registration Country : USA

blank

22

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : BACTRIM

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 17560

Regulatory Info : DISCN

Registration Country : USA

blank

23

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : BACTRIM PEDIATRIC

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 17560

Regulatory Info : DISCN

Registration Country : USA

blank

24

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : BACTRIM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 80MG/ML;16MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 18374

Regulatory Info : DISCN

Registration Country : USA

blank

25

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1982-01-01

Application Number : 18242

Regulatory Info : DISCN

Registration Country : USA

blank

26

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1982-01-01

Application Number : 18242

Regulatory Info : DISCN

Registration Country : USA

blank

27

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML

Packaging :

Approval Date : 1983-01-28

Application Number : 18812

Regulatory Info : DISCN

Registration Country : USA

blank

28

Fi Europe 2024
Not Confirmed
arrow
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 200MG/5ML;40MG/5ML

Packaging :

Approval Date : 1983-06-10

Application Number : 18812

Regulatory Info : DISCN

Registration Country : USA

blank

29

HEATHER

Country
Fi Europe 2024
Not Confirmed
arrow

HEATHER

Country
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG;80MG

Packaging :

Approval Date : 1984-08-10

Application Number : 18946

Regulatory Info : DISCN

Registration Country : USA

blank

30

HEATHER

Country
Fi Europe 2024
Not Confirmed
arrow

HEATHER

Country
arrow
Fi Europe 2024
Not Confirmed

SULFAMETHOXAZOLE; TRIMETHOPRIM

Brand Name : SULFAMETHOXAZOLE AND TRIMETHOPRIM

Dosage Form : TABLET;ORAL

Dosage Strength : 800MG;160MG

Packaging :

Approval Date : 1984-08-10

Application Number : 18946

Regulatory Info : DISCN

Registration Country : USA

blank