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01 2SANOFI AVENTIS US

02 1MANKIND PHARMA

03 2ABRAXIS PHARM

04 1ACCORD HLTHCARE

05 1AM REGENT

06 1AMNEAL PHARMS CO

07 3ANI PHARMS

08 1AREVA PHARMS

09 1ASPIRO

10 1ASTRAZENECA

11 3AUROBINDO PHARMA LTD

12 1AVET LIFESCIENCES

13 1BAXTER HLTHCARE CORP

14 2CHARTWELL RX

15 4EPIC PHARMA LLC

16 3ESJAY PHARMA

17 1EUGIA PHARMA

18 1FRESENIUS KABI USA

19 1GLAND

20 3GRAVITI PHARMS

21 7HIKMA

22 5HOSPIRA

23 2IGI LABS INC

24 3INTL MEDICATION

25 3IPCA LABS LTD

26 2KALAPHARM

27 3LEADING

28 1MARSAM PHARMS LLC

29 1MEITHEAL

30 3NORVIUM BIOSCIENCE

31 1PHARMOBEDIENT CNSLTG

32 3PRINSTON INC

33 1SABA ILAC SANAYIVE

34 1SAGENT

35 1SCPHARMACEUTICALS

36 2SMITH AND NEPHEW

37 1SQ INNOVATION, INC

38 4SUN PHARM INDS INC

39 2SUN PHARM INDUSTRIES

40 2SUPERPHARM

41 3VALIDUS PHARMS

42 4WARNER CHILCOTT

43 6WATSON LABS

44 2WATSON LABS TEVA

45 1WOCKHARDT BIO AG

46 1WYETH AYERST

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PharmaCompass

01

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Dosage Strength : 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AP

FUROSEMIDE

Brand Name : FUROSEMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/ML

Approval Date : 2022-12-16

Application Number : 216860

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

Company Banner

03

  • 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

04

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
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 :

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05

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
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 :

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06

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
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

07

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
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

08

KY/TN Water Professionals
Not Confirmed
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arrow
KY/TN Water Professionals
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

09

KY/TN Water Professionals
Not Confirmed
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arrow
KY/TN Water Professionals
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

10

KY/TN Water Professionals
Not Confirmed
arrow
arrow
KY/TN Water Professionals
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

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