Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 47Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 2SANOFI AVENTIS US

02 2ABRAXIS PHARM

03 1ACCORD HLTHCARE

04 1AM REGENT

05 1AMNEAL PHARMS CO

06 3ANI PHARMS

07 1AREVA PHARMS

08 1ASPIRO

09 1ASTRAZENECA

10 1AVET LIFESCIENCES

11 1BAXTER HLTHCARE CORP

12 2CHARTWELL RX

13 4EPIC PHARMA LLC

14 3ESJAY PHARMA

15 1EUGIA PHARMA

16 1FRESENIUS KABI USA

17 1GLAND PHARMA LTD

18 3GRAVITI PHARMS

19 7HIKMA

20 5HOSPIRA

21 2IGI LABS INC

22 3INTL MEDICATION

23 3IPCA LABS LTD

24 2KALAPHARM

25 3LEADING

26 1MANKIND PHARMA

27 1MARSAM PHARMS LLC

28 1MEITHEAL

29 1MYLAN

30 2NORVIUM BIOSCIENCE

31 1PHARMOBEDIENT CNSLTG

32 3PRINSTON INC

33 1SABA ILAC SANAYIVE

34 1SAGENT

35 1SCPHARMACEUTICALS

36 2SMITH AND NEPHEW

37 4SUN PHARM INDS INC

38 2SUN PHARM INDUSTRIES

39 2SUPERPHARM

40 3VALIDUS PHARMS

41 4WARNER CHILCOTT

42 6WATSON LABS

43 2WATSON LABS TEVA

44 1WOCKHARDT

45 1WYETH AYERST

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

arrow
BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : Yes

TE Code :

FUROSEMIDE

Brand Name : LASIX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 16363

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

02

arrow
BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

FUROSEMIDE

Brand Name : LASIX

Dosage Form : SOLUTION;ORAL

Dosage Strength : 10MG/ML

Approval Date : 1982-01-01

Application Number : 17688

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

03

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : FUROSEMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Approval Date : 1982-05-14

Application Number : 18369

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

04

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : FUROSEMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Approval Date : 1982-05-14

Application Number : 18369

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

05

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : FUROSEMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/ML

Approval Date : 1982-01-01

Application Number : 18025

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

06

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : FUROSEMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/ML

Approval Date : 1982-01-01

Application Number : 18267

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

blank

07

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : LASIX

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Approval Date : 1982-01-01

Application Number : 16273

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

08

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : LASIX

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Approval Date : 1982-01-01

Application Number : 16273

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

09

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : LASIX

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG

Approval Date : 1982-01-01

Application Number : 16273

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

10

SUPERPHARM

Country
BioAsia
Not Confirmed
arrow

SUPERPHARM

Country
arrow
BioAsia
Not Confirmed

FUROSEMIDE

Brand Name : FUROSEMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Approval Date : 1983-02-10

Application Number : 18370

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank