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01 3SANOFI AVENTIS US

02 3ACCORD HLTHCARE

03 3ACTAVIS LABS FL INC

04 3AUROBINDO PHARMA LTD

05 3CARLSBAD

06 3CHARTWELL MOLECULAR

07 2CHARTWELL RX

08 3DR REDDYS LABS LTD

09 3EPIC PHARMA LLC

10 3HIKMA PHARMS

11 6MICRO LABS

12 3MYLAN

13 4PRINSTON INC

14 3QUAGEN

15 2RANBAXY

16 4RANBAXY LABS LTD

17 3REGCON HOLDINGS

18 5SB PHARMCO

19 3SENORES PHARMS

20 2TAKEDA PHARMS USA

21 5TEVA PHARMS USA

22 3WATSON LABS

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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 :

GLIMEPIRIDE

Brand Name : AMARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1995-11-30

Application Number : 20496

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

02

  • 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 :

GLIMEPIRIDE

Brand Name : AMARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1995-11-30

Application Number : 20496

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi 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 : Yes

TE Code :

GLIMEPIRIDE

Brand Name : AMARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1995-11-30

Application Number : 20496

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

04

SB PHARMCO

U.S.A
34th NZW-Hamburg
Not Confirmed
arrow

SB PHARMCO

U.S.A
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Brand Name : AVANDARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2005-11-23

Application Number : 21700

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

SB PHARMCO

U.S.A
34th NZW-Hamburg
Not Confirmed
arrow

SB PHARMCO

U.S.A
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Brand Name : AVANDARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2005-11-23

Application Number : 21700

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

06

SB PHARMCO

U.S.A
34th NZW-Hamburg
Not Confirmed
arrow

SB PHARMCO

U.S.A
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Brand Name : AVANDARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2005-11-23

Application Number : 21700

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

SB PHARMCO

U.S.A
34th NZW-Hamburg
Not Confirmed
arrow

SB PHARMCO

U.S.A
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Brand Name : AVANDARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG;8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2007-03-30

Application Number : 21700

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

SB PHARMCO

U.S.A
34th NZW-Hamburg
Not Confirmed
arrow

SB PHARMCO

U.S.A
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Brand Name : AVANDARYL

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG;8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2007-03-30

Application Number : 21700

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

34th NZW-Hamburg
Not Confirmed
arrow
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : DUETACT

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG;30MG

Approval Date : 2006-07-28

Application Number : 21925

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

10

34th NZW-Hamburg
Not Confirmed
arrow
arrow
34th NZW-Hamburg
Not Confirmed

GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : DUETACT

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG;30MG

Approval Date : 2006-07-28

Application Number : 21925

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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