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01 4STRIDES PHARMA

02 2ACTAVIS MID ATLANTIC

03 1AIPING PHARM INC

04 2AIZANT

05 2AM THERAP

06 1AMNEAL PHARMS

07 2AMNEAL PHARMS CO

08 5APOTEX INC

09 2ARMSTRONG PHARMS

10 2AUROBINDO PHARMA LTD

11 2BAUSCH

12 2BOEHRINGER INGELHEIM

13 1CHARTWELL MOLECULAR

14 4CHARTWELL RX

15 2CIPLA

16 4COPLEY PHARM

17 1COSETTE

18 2DASH PHARMS NATCO

19 1EPIC PHARMA LLC

20 1GENPHARM

21 8GLAXOSMITHKLINE

22 2HIBROW HLTHCARE

23 1HIKMA

24 1IVAX SUB TEVA PHARMS

25 1KINDEVA

26 1LANDELA PHARM

27 2LEXENPHARM

28 4LUOXIN AUROVITAS

29 1LUPIN

30 1MOVA

31 2MURO

32 6NEPHRON

33 4NORVIUM BIOSCIENCE

34 1PADAGIS US

35 3PLIVA

36 1QUAGEN

37 4RISING

38 4RITEDOSE CORP

39 1ROXANE

40 1SANDOZ

41 7SCHERING

42 1SENTISS

43 2SUN PHARM

44 2SUN PHARM INDUSTRIES

45 7TEVA

46 3TEVA BRANDED PHARM

47 2TEVA PHARMS

48 2UCB INC

49 2VIRTUS PHARM

50 2WARNER CHILCOTT

51 7WATSON LABS

52 1WATSON LABS INC

53 1WATSON LABS TEVA

54 1WOCKHARDT EU OPERATN

55 2ZYDUS PHARMS

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PharmaCompass

01

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Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code :

ALBUTEROL SULFATE

Brand Name : ALBUTEROL SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 4MG BASE

Approval Date : 1989-12-20

Application Number : 72860

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

02

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Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code :

ALBUTEROL SULFATE

Brand Name : ALBUTEROL SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Approval Date : 1989-12-20

Application Number : 72860

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

03

arrow
Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code :

ALBUTEROL SULFATE

Brand Name : VOSPIRE ER

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 4MG BASE

Approval Date : 2002-09-26

Application Number : 76130

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

04

arrow
Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code :

ALBUTEROL SULFATE

Brand Name : VOSPIRE ER

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 8MG BASE

Approval Date : 2002-09-26

Application Number : 76130

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

05

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

ALBUTEROL

Brand Name : PROVENTIL

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.09MG/INH

Approval Date : 1982-01-01

Application Number : 17559

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

06

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

ALBUTEROL SULFATE

Brand Name : PROVENTIL

Dosage Form : TABLET;ORAL

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

Approval Date : 1982-05-07

Application Number : 17853

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

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

ALBUTEROL SULFATE

Brand Name : PROVENTIL

Dosage Form : TABLET;ORAL

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

Approval Date : 1982-05-07

Application Number : 17853

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

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

ALBUTEROL SULFATE

Brand Name : PROVENTIL

Dosage Form : SYRUP;ORAL

Dosage Strength : EQ 2MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1983-01-19

Application Number : 18062

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

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

ALBUTEROL

Brand Name : VENTOLIN

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.09MG/INH

Approval Date : 1982-01-01

Application Number : 18473

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

10

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

ALBUTEROL SULFATE

Brand Name : VENTOLIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Approval Date : 1986-07-10

Application Number : 19112

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank