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01 2SANOFI AVENTIS US

02 2ABRAXIS PHARM

03 1ACCORD HLTHCARE

04 1AM REGENT

05 1AMNEAL PHARMS CO

06 3ANI PHARMS

07 1AREVA PHARMS

08 1ASTRAZENECA

09 1AVET LIFESCIENCES

10 1BAXTER HLTHCARE CORP

11 2CHARTWELL RX

12 4EPIC PHARMA LLC

13 3ESJAY PHARMA

14 1EUGIA PHARMA

15 1FRESENIUS KABI USA

16 1GLAND PHARMA LTD

17 3GRAVITI PHARMS

18 7HIKMA

19 5HOSPIRA

20 2IGI LABS INC

21 3INTL MEDICATION

22 3IPCA LABS LTD

23 2KALAPHARM

24 3LEADING

25 1MANKIND PHARMA

26 1MARSAM PHARMS LLC

27 1MEITHEAL

28 3MYLAN

29 1PHARMOBEDIENT CNSLTG

30 3PRINSTON INC

31 1SABA ILAC SANAYIVE

32 1SAGENT

33 1SCPHARMACEUTICALS

34 2SMITH AND NEPHEW

35 4SUN PHARM INDS INC

36 2SUN PHARM INDUSTRIES

37 2SUPERPHARM

38 3VALIDUS PHARMS

39 4WARNER CHILCOTT

40 6WATSON LABS

41 2WATSON LABS TEVA

42 1WOCKHARDT

43 1WYETH AYERST

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PharmaCompass

01

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Pharma, Lab & Chemical Expo
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Dosage Strength : 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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arrow
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
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
Pharma, Lab & Chemical Expo
Not Confirmed
arrow

SUPERPHARM

Country
arrow
Pharma, Lab & Chemical Expo
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