Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 37Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 4Dr. Reddy's Laboratories

02 4Strides Pharma Science

03 4Granules India Limited

04 4ATNAHS PHARMA UK LIMITED

05 7Actavis Inc

06 3Adamed Pharma

07 1Aeon Formulations Private Limited

08 4Amneal Pharmaceuticals

09 1Antibiotice SA

10 2Apotex Inc

11 1Aralez Pharmaceuticals

12 1Ascent Innovative Medicines

13 5Aurobindo Pharma Limited

14 12Bayer AG

15 4Biofarma Pharmaceutical Industry and Commerce Inc

16 1Bionpharma

17 1Catalent Pharma Solutions

18 2Contract Pharmacal Corporation

19 1CorePharma, LLC

20 2Currax

21 2Glenmark Pharmaceuticals

22 1Grup Farma

23 2Hamilton

24 1Hetero Drugs

25 2Hikma Pharmaceuticals

26 1Holden Medical Laboratories Pvt. Ltd

27 2IVAX Pharmaceuticals Inc

28 1LNK

29 1Madras Pharmaceuticals

30 1Marksans Pharma

31 1Meda OTC AB,

32 1Myungmoon Pharm. Co., LTD.

33 2NORVIUM BIOSCIENCE

34 2Noripharma

35 1Novelgenix

36 1PL Developments

37 1PLD ACQUISITIONS

38 2PRO DOC LIMITEE

39 1PURACAP PHARM

40 2PUREPAC PHARM

41 1Par Pharmaceutical

42 1Patheon

43 1Patheon Softgels BV

44 3Perrigo Company plc

45 4Pharmascience Inc.

46 2Pliva Hrvatska

47 2ROXANE

48 1Rising Pharmaceuticals Inc

49 4Sandoz B2B

50 2ScieGen Pharmaceuticals

51 1Seoul Pharma Co Ltd

52 4Sun Pharmaceutical Industries Limited

53 2T.M.Thakore Pharmaceutical Laboratories

54 3TWi Pharmaceuticals

55 8Teva Pharmaceutical Industries

56 2Umedica Laboratories

57 1Whanin Pharmaceutical

58 2World Medicine

59 3XYZ Pharma

60 2Yichang Humanwell Pharmaceutical

61 2Zim Laboratories

62 5Blank

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : OTC

Registration Country : USA

NAPROXEN SODIUM

Brand Name : NAPROXEN SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 220MG

Packaging :

Approval Date : 1998-07-28

Application Number : 75168

Regulatory Info : OTC

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

NAPROXEN SODIUM

Brand Name : NAPROXEN SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2022-08-17

Application Number : 215472

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

Regulatory Info : OTC

Registration Country : USA

NAPROXEN SODIUM

Brand Name : NAPROXEN SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 220MG

Packaging :

Approval Date : 2011-09-20

Application Number : 91353

Regulatory Info : OTC

Registration Country : USA

Granules India

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : OTC

Registration Country : USA

NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE

Brand Name : NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 220MG;120MG

Packaging :

Approval Date : 2006-09-27

Application Number : 77381

Regulatory Info : OTC

Registration Country : USA

Dr Reddy Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Esomeprazole Magnesium; Naproxen Sodium

Brand Name :

Dosage Form : Oral Solid Dosage Form

Dosage Strength : 20MG; 375MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Esomeprazole Magnesium; Naproxen Sodium

Brand Name :

Dosage Form : Oral Solid Dosage Form

Dosage Strength : 20MG; 500MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Naproxen Sodium

Brand Name :

Dosage Form : Tablet

Dosage Strength : 250MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

08

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Naproxen Sodium

Brand Name :

Dosage Form : Tablet

Dosage Strength : 500MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

09

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Naproxen Sodium

Brand Name :

Dosage Form : Soft Gel Capsule

Dosage Strength : 220MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

10

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

Regulatory Info : OTC

Registration Country : USA

DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

Brand Name : NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;220MG

Packaging :

Approval Date : 2020-09-24

Application Number : 213663

Regulatory Info : OTC

Registration Country : USA

Granules India

11

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

Regulatory Info : TP, ODMF

Registration Country : India

Naproxen Sodium

Brand Name : Compresso NAP 73.3

Dosage Form : Pellets

Dosage Strength : 73.3%

Packaging :

Approval Date :

Application Number :

Regulatory Info : TP, ODMF

Registration Country : India

Granules India

12

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

Regulatory Info : ROW, US

Registration Country : India

Naproxen Sodium

Brand Name :

Dosage Form : Immediate Release Tablet

Dosage Strength : 220MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : ROW, US

Registration Country : India

Granules India

13

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : ANAPROX

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 18164

Regulatory Info : DISCN

Registration Country : USA

blank

14

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : ANAPROX DS

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 1987-09-30

Application Number : 18164

Regulatory Info : RX

Registration Country : USA

blank

15

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : ALEVE

Dosage Form : TABLET;ORAL

Dosage Strength : 220MG

Packaging :

Approval Date : 1994-01-11

Application Number : 20204

Regulatory Info : OTC

Registration Country : USA

blank

16

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE

Brand Name : ALEVE-D SINUS & COLD

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 220MG;120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-11-29

Application Number : 21076

Regulatory Info : DISCN

Registration Country : USA

blank

17

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : NAPROXEN SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2006-02-17

Application Number : 21920

Regulatory Info : OTC

Registration Country : USA

blank

18

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : NAPRELAN

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 375MG BASE

Packaging :

Approval Date : 1996-01-05

Application Number : 20353

Regulatory Info : RX

Registration Country : USA

blank

19

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : NAPRELAN

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 1996-01-05

Application Number : 20353

Regulatory Info : RX

Registration Country : USA

blank

20

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NAPROXEN SODIUM

Brand Name : NAPRELAN

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 750MG BASE

Packaging :

Approval Date : 1996-01-05

Application Number : 20353

Regulatory Info : RX

Registration Country : USA

blank