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Naproxen Sodium
Canada

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

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Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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xyz-pharma-m-2024-10-07

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With Fermion, start the journey of your innovative API.

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Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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xyz-pharma-m-2024-10-07

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Naproxen Sodium

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

31 API Suppliers, 22 USDMF, 8 CEP/COS, 5 EU WC, 34 KDMF, 11 NDC API, 9 Listed Suppliers, $ API Reference Price

31 API Suppliers
22 USDMF
8 CEP/COS
5 EU WC
34 KDMF
11 NDC API
9 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

6 Drugs in Development

6 Drugs in Development

FINISHED DOSAGE FORMULATIONS

152 FDF Dossiers, 85 FDA Orange Book, 11 Europe, 18 Canada, 4 South Africa, 34 Listed Dossiers

152 FDF Dossiers
85 FDA Orange Book
11 Europe
18 Canada
4 South Africa
34 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 500MG BASE, TABLET;ORAL - 220MG, TABLET, EXTENDED RELEASE;ORAL - EQ 375MG BASE, TABLET, EXTENDED RELEASE;ORAL - EQ 500MG BASE, TABLET, EXTENDED RELEASE;ORAL - EQ 750MG BASE, CAPSULE;ORAL - EQ 200MG BASE, TABLET;ORAL - 500MG;EQ 85MG BASE, TABLET;ORAL - 60MG;EQ 10MG BASE

TABLET;ORAL - EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 500MG BASE
TABLET;ORAL - 220MG
TABLET, EXTENDED RELEASE;ORAL - EQ 375MG BASE
TABLET, EXTENDED RELEASE;ORAL - EQ 500MG BASE
TABLET, EXTENDED RELEASE;ORAL - EQ 750MG BASE
CAPSULE;ORAL - EQ 200MG BASE
TABLET;ORAL - 500MG;EQ 85MG BASE
TABLET;ORAL - 60MG;EQ 10MG BASE

RELATED EXCIPIENT COMPANIES

3 Evonik, 4 Rochem International Inc, 19 SPI Pharma, 2 Seqens, 9 DKSH, 8 Faran Shimi Pharmaceutical, 11 Boai NKY Pharmaceuticals Ltd, 14 Gangwal Healthcare, 11 Nanjing Well Pharmaceutical, 2 Pfanstiehl, 4 ACG Worldwide, 11 Actylis, 2 Aeon Procare, 1 Alcedo Pharmachem, 9 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 33 BASF, 3 Clariant, 17 Corel Pharma Chem, 6 DFE Pharma, 2 Finar, 13 Gangwal Chemicals, 11 Ideal Cures Pvt Ltd, 5 Ingredion Pharma Solutions, 33 Kerry, 4 Kima Chemical, 6 Lonza Capsugel, 20 Microlex e.U, 1 Nanjing Bold Chemical, 2 Nomisma Healthcare, 4 Novo Excipients, 4 Pharmatrans-Sanaq, 9 Pluviaendo, 4 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 2 Qualicaps, 38 Roquette, 13 Seppic, 7 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shanghai Welltone Material Technology Co., Ltd, 2 Shijiazhuang Huaxu Pharmaceutical, 12 Sigachi Industries, 3 The Dow Chemical Company, 3 Ulanqab Kema New Material, 1 Valens Pharmachem, 4 Vasa Pharmachem, 1 Vertellus, 1 Zhejiang Huakang Pharmaceutical

EXCIPIENTS BY APPLICATIONS

105 Fillers, Diluents & Binders, 65 Coating Systems & Additives, 48 Direct Compression, 44 Controlled & Modified Release, 43 Thickeners and Stabilizers, 42 Disintegrants & Superdisintegrants, 36 Solubilizers, 31 Granulation, 30 Film Formers & Plasticizers, 30 Parenteral, 25 Taste Masking, 24 Topical, 24 Lubricants & Glidants, 22 Co-Processed Excipients, 19 Chewable & Orodispersible Aids, 9 Empty Capsules, 9 API Stability Enhancers, 9 Emulsifying Agents, 9 Rheology Modifiers, 5 Surfactant & Foaming Agents, 5 Coloring Agents, 4 Vegetarian Capsules, 1 Soft Gelatin

105 Fillers, Diluents & Binders
65 Coating Systems & Additives
48 Direct Compression
44 Controlled & Modified Release
43 Thickeners and Stabilizers
42 Disintegrants & Superdisintegrants
36 Solubilizers
31 Granulation
30 Film Formers & Plasticizers
30 Parenteral
25 Taste Masking
24 Topical
24 Lubricants & Glidants
22 Co-Processed Excipients
19 Chewable & Orodispersible Aids
9 Empty Capsules
9 API Stability Enhancers
9 Emulsifying Agents
9 Rheology Modifiers
5 Surfactant & Foaming Agents
5 Coloring Agents
4 Vegetarian Capsules
1 Soft Gelatin

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow, 44 NEWS #PharmaBuzz

1 DATA COMPILATION #PharmaFlow
44 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

3 US Medicaid Prescriptions, 8 Finished Drug Prices

3 US Medicaid Prescriptions
8 Finished Drug Prices

MARKET PLACE

38 APIs, 2 FDF Dossiers

38 APIs
2 FDF Dossiers

PATENTS & EXCLUSIVITIES

12 US Patents, 2 Health Canada Patents

12 US Patents
2 Health Canada Patents

REF. STANDARDS & IMPURITIES

3 EDQM, 1 USP, 1 Others

3 EDQM
1 USP
1 Others

ANALYTICAL

1 BioAnalytical Methods

1 BioAnalytical Methods

$ API Ref.Price (USD/KG) : 37 Xls

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18 All

01 2APOTEX INC

02 1ARALEZ PHARMACEUTICALS CANADA INC

03 2ATNAHS PHARMA UK LIMITED

04 5BAYER INC

05 2PHARMASCIENCE INC

06 2PRO DOC LIMITEE

07 2Pharmascience Inc.

08 2TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

18 All

01 16NAPROXEN SODIUM

02 2Naproxen Sodium

filter Dosage Form Reset all filters

18 All

01 3CAPSULE

02 15TABLET

filter Brand Name Reset all filters

18 All

01 1ALEVE BACK AND BODY PAIN

02 1ALEVE CAPLETS

03 1ALEVE LIQUID GELS

04 1ALEVE NIGHTTIME

05 1ANAPROX

06 1ANAPROX DS

07 1APO-NAPRO-NA

08 1APO-NAPRO-NA DS

09 1MAXIDOL LIQUID GELS

10 2NAPROXEN

11 2NAPROXEN MENSTRUAL PAIN RELIEF

12 1NAPROXEN-NA

13 1NAPROXEN-NA DF

14 1SUVEXX

15 1TEVA-NAPROXEN SODIUM

16 1TEVA-NAPROXEN SODIUM DS

List of Suppliers

Product Main Page

01

APOTEX INC

Pharma, Lab & Chemical Expo

Not Confirmed

APOTEX INC

Pharma, Lab & Chemical Expo

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : APO-NAPRO-NA

Dosage Form : TABLET

Dosage Strength : 275MG

Packaging : 100/500

Approval Date :

Application Number : 784354

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

APOTEX INC

Pharma, Lab & Chemical Expo

Not Confirmed

APOTEX INC

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : APO-NAPRO-NA DS

Dosage Form : TABLET

Dosage Strength : 550MG

Packaging : 100 & 500 TABLETS

Approval Date :

Application Number : 1940309

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

03

ATNAHS PHARMA UK LIMITED

Pharma, Lab & Chemical Expo

Not Confirmed

ATNAHS PHARMA UK LIMITED

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : ANAPROX DS

Dosage Form : TABLET

Dosage Strength : 550MG

Packaging : 100

Approval Date :

Application Number : 2162717

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

ATNAHS PHARMA UK LIMITED

Pharma, Lab & Chemical Expo

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ATNAHS PHARMA UK LIMITED

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : ANAPROX

Dosage Form : TABLET

Dosage Strength : 275MG

Packaging : 100

Approval Date :

Application Number : 2162725

Regulatory Info : Prescription

Registration Country : Canada

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Digital Content

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05

Pharmascience Inc.

Pharma, Lab & Chemical Expo

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Pharmascience Inc.

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : OTC

Registration Country : Canada

Naproxen Sodium

Brand Name : NAPROXEN

Dosage Form : TABLET

Dosage Strength : 220MG

Packaging : 24/100

Approval Date :

Application Number :

Regulatory Info : OTC

Registration Country : Canada

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Product Web Link

Digital Content

06

Pharmascience Inc.

Pharma, Lab & Chemical Expo

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Pharmascience Inc.

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : OTC

Registration Country : Canada

Naproxen Sodium

Brand Name : NAPROXEN MENSTRUAL PAIN RELIEF

Dosage Form : TABLET

Dosage Strength : 220MG

Packaging : 24/30/50

Approval Date :

Application Number :

Regulatory Info : OTC

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

07

PRO DOC LIMITEE

Pharma, Lab & Chemical Expo

Not Confirmed

PRO DOC LIMITEE

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : NAPROXEN-NA DF

Dosage Form : TABLET

Dosage Strength : 550MG

Packaging : 100/500

Approval Date :

Application Number : 2153386

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

08

PRO DOC LIMITEE

Pharma, Lab & Chemical Expo

Not Confirmed

PRO DOC LIMITEE

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : NAPROXEN-NA

Dosage Form : TABLET

Dosage Strength : 275MG

Packaging :

Approval Date :

Application Number : 887056

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

09

TEVA CANADA LIMITED

Pharma, Lab & Chemical Expo

Not Confirmed

TEVA CANADA LIMITED

Pharma, Lab & Chemical Expo

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : TEVA-NAPROXEN SODIUM

Dosage Form : TABLET

Dosage Strength : 275MG

Packaging : 100/500/1000

Approval Date :

Application Number : 778389

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

10

TEVA CANADA LIMITED

Pharma, Lab & Chemical Expo

Not Confirmed

TEVA CANADA LIMITED

Pharma, Lab & Chemical Expo

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Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NAPROXEN SODIUM

Brand Name : TEVA-NAPROXEN SODIUM DS

Dosage Form : TABLET

Dosage Strength : 550MG

Packaging : 100/500

Approval Date :

Application Number : 2026600

Regulatory Info : Prescription

Registration Country : Canada

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Product Web Link

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