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01 4Sanofi

02 1Allergan Aesthetics

03 3Actavis Inc

04 2Ailex Pharma

05 2Alfasigma

06 1Apotex Inc

07 1Appasamy Associates

08 1Aurobindo Pharma Limited

09 1Aurolab

10 3Bausch & Lomb Incorporated

11 1Biodeal Pharmaceuticals

12 1Bruschettini

13 1FDC

14 2Farmak JSC

15 1Fera Pharmaceuticals, LLC

16 1GENERA PHARMS

17 1HH AND P

18 2Hanlim Pharmaceuticals Inc

19 1Hikma Pharmaceuticals

20 3ITALCHIMICI SpA

21 1Ideal Trade Links Uab

22 1Laboratoires Thea

23 1Lupin Ltd

24 2MARVECSPHARMA SERVICES Srl

25 2Micro Labs Limited

26 1Mirpharm

27 1Novartis Pharmaceuticals Corporation

28 4ORIFARM GROUP AS

29 1Opella Healthcare Group

30 2Pannon

31 1Pendopharm

32 1Perrigo Company plc

33 3Pfizer Inc

34 1Pharmascience Inc.

35 1Prestige Consumer Healthcare

36 1ROXANE

37 1Raha Pharmaceutical Co

38 1Rekah Pharmaceutical

39 1Rising Pharmaceuticals Inc

40 1S.C. Rompharm Company SRL

41 1SIFI

42 2STADA Arzneimittel

43 2Sandoz B2B

44 4Santen Pharmaceutical

45 1ScieGen Pharmaceuticals

46 1Teva Pharmaceutical Industries

47 1UCB Pharma S.A

48 2Unither Pharmaceuticals

49 1Viatris

50 1Winston Medical Supply

51 1Wockhardt

52 6World Medicine

53 1Blank

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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.

Regulatory Info : DISCN

Registration Country : USA

CROMOLYN SODIUM

Brand Name : INTAL

Dosage Form : CAPSULE;INHALATION

Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 16990

Regulatory Info : DISCN

Registration Country : USA

Sanofi Company Banner

02

CROMOLYN SODIUM

Brand Name : OPTICROM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1984-10-03

Application Number : 18155

Regulatory Info : DISCN

Registration Country : USA

Abbvie CB

03

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : Italy

Cromolyn Sodium

Brand Name : Lomudal

Dosage Form :

Dosage Strength : Coll 10 Ml 4%  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : Italy

Cromolyn Sodium

Brand Name : Lomudal

Dosage Form :

Dosage Strength : Nasal Soluz 30 Ml 4 % + Nebulizer  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : Italy

Cromolyn Sodium

Brand Name : Lomudal

Dosage Form :

Dosage Strength : 24 Vials 20 Mg 2 Ml Aerosol  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

06

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 5.2MG/SPRAY

Packaging :

Approval Date : 2001-07-26

Application Number : 74800

Regulatory Info : DISCN

Registration Country : USA

blank

07

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 10MG/ML

Packaging :

Approval Date : 1999-07-19

Application Number : 75067

Regulatory Info : DISCN

Registration Country : USA

blank

08

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 10MG/ML

Packaging :

Approval Date : 1994-04-26

Application Number : 74209

Regulatory Info : DISCN

Registration Country : USA

blank

09

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROLOM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 4%

Packaging :

Approval Date : 1995-01-30

Application Number : 74443

Regulatory Info : DISCN

Registration Country : USA

blank

10

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 10MG/ML

Packaging :

Approval Date : 2002-04-30

Application Number : 75333

Regulatory Info : DISCN

Registration Country : USA

blank

11

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : INTAL

Dosage Form : SOLUTION;INHALATION

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

Packaging :

Approval Date : 1982-05-28

Application Number : 18596

Regulatory Info : DISCN

Registration Country : USA

blank

12

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : INTAL

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.8MG/INH

Packaging :

Approval Date : 1985-12-05

Application Number : 18887

Regulatory Info : DISCN

Registration Country : USA

blank

13

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOPTIC

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 4%

Packaging :

Approval Date : 1999-04-27

Application Number : 75088

Regulatory Info : DISCN

Registration Country : USA

blank

14

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : NASALCROM

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 5.2MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1997-01-03

Application Number : 20463

Regulatory Info : DISCN

Registration Country : USA

blank

15

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 10MG/ML

Packaging :

Approval Date : 1999-09-30

Application Number : 75175

Regulatory Info : DISCN

Registration Country : USA

blank

16

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 4%

Packaging :

Approval Date : 1999-06-16

Application Number : 75282

Regulatory Info : RX

Registration Country : USA

blank

17

IPPE
Not Confirmed
arrow
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 4%

Packaging :

Approval Date : 1998-04-29

Application Number : 74706

Regulatory Info : DISCN

Registration Country : USA

blank

18

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : CROMOLYN SODIUM

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 10MG/ML

Packaging :

Approval Date : 2000-01-18

Application Number : 75271

Regulatory Info : RX

Registration Country : USA

blank

19

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : GASTROCROM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1989-12-22

Application Number : 19188

Regulatory Info : DISCN

Registration Country : USA

blank

20

IPPE
Not Confirmed
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IPPE
Not Confirmed

CROMOLYN SODIUM

Brand Name : GASTROCROM

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 100MG/5ML

Packaging :

Approval Date : 1996-02-29

Application Number : 20479

Regulatory Info : RX

Registration Country : USA

blank