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Wymox
Canada

AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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Wymox

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

107 API Suppliers, 39 USDMF, 32 CEP/COS, 5 JDMF, 2 EU WC, 41 KDMF, 18 NDC API, 4 VMF, 27 Listed Suppliers, $ API Reference Price

107 API Suppliers
39 USDMF
32 CEP/COS
5 JDMF
2 EU WC
41 KDMF
18 NDC API
4 VMF
27 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

54 Drugs in Development

54 Drugs in Development

INTERMEDIATES

2 Intermediate Suppliers

2 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

1966 FDF Dossiers, 208 FDA Orange Book, 894 Europe, 114 Canada, 127 Australia, 223 South Africa, 400 Listed Dossiers

1966 FDF Dossiers
208 FDA Orange Book
894 Europe
114 Canada
127 Australia
223 South Africa
400 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - 250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 500MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, FOR SUSPENSION;ORAL - 125MG/5ML;EQ 31.25MG BASE/5ML, FOR SUSPENSION;ORAL - 250MG/5ML;EQ 62.5MG BASE/5ML, TABLET;ORAL - 875MG;EQ 125MG BASE, FOR SUSPENSION;ORAL - 200MG/5ML;EQ 28.5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, FOR SUSPENSION;ORAL - 400MG/5ML;EQ 57MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, FOR SUSPENSION;ORAL - 600MG/5ML;EQ 42.9MG BASE/5ML, CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL - 500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, FOR SUSPENSION;ORAL - 200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, FOR SUSPENSION;ORAL - 400MG/5ML, TABLET, EXTENDED RELEASE;ORAL - 1GM;EQ 62.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 775MG, CAPSULE, TABLET, CAPSULE, DELAYED RELEASE;ORAL - 500MG,N/A,N/A;N/A,500MG,N/A;N/A,N/A,20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET;ORAL - 250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 500MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
FOR SUSPENSION;ORAL - 125MG/5ML;EQ 31.25MG BASE/5ML
FOR SUSPENSION;ORAL - 250MG/5ML;EQ 62.5MG BASE/5ML
TABLET;ORAL - 875MG;EQ 125MG BASE
FOR SUSPENSION;ORAL - 200MG/5ML;EQ 28.5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
FOR SUSPENSION;ORAL - 400MG/5ML;EQ 57MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
FOR SUSPENSION;ORAL - 600MG/5ML;EQ 42.9MG BASE/5ML
CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL - 500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
FOR SUSPENSION;ORAL - 200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
FOR SUSPENSION;ORAL - 400MG/5ML
TABLET, EXTENDED RELEASE;ORAL - 1GM;EQ 62.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 775MG
CAPSULE, TABLET, CAPSULE, DELAYED RELEASE;ORAL - 500MG,N/A,N/A;N/A,500MG,N/A;N/A,N/A,20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

RELATED EXCIPIENT COMPANIES

1 Rochem International Inc, 1 SPI Pharma, 1 Pharm-RX Chemical, 3 Gangwal Healthcare, 1 Kirsch Pharma, 1 ACG Worldwide, 3 Actylis, 5 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 8 BASF, 2 CD Formulation, 10 Corel Pharma Chem, 3 DFE Pharma, 1 Esteem Industries, 1 Finar, 6 Gangwal Chemicals, 4 Ideal Cures, 1 Ingredion Pharma Solutions, 10 Kerry, 2 Keval Exports, 3 Kima Chemical, 6 Lonza Capsugel, 8 Microlex e.U, 2 Nitika Pharmaceutical Specialities, 2 Nomisma Healthcare, 1 Novo Excipients, 2 Pharmatrans-Sanaq, 1 Pluviaendo, 3 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Qualicaps, 11 Roquette, 6 Seppic, 3 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 9 Sigachi Industries, 3 Silverline Chemicals, 2 The Dow Chemical Company, 3 Vasa Pharmachem

EXCIPIENTS BY APPLICATIONS

37 Coating Systems & Additives, 22 Fillers, Diluents & Binders, 19 Controlled & Modified Release, 18 Thickeners and Stabilizers, 14 Disintegrants & Superdisintegrants, 11 Lubricants & Glidants, 9 Granulation, 9 Direct Compression, 8 Topical, 7 Co-Processed Excipients, 6 Film Formers & Plasticizers, 5 Empty Capsules, 5 API Stability Enhancers, 5 Taste Masking, 5 Solubilizers, 4 Chewable & Orodispersible Aids, 4 Vegetarian Capsules, 3 Emulsifying Agents, 3 Rheology Modifiers, 2 Coloring Agents, 1 Parenteral

37 Coating Systems & Additives
22 Fillers, Diluents & Binders
19 Controlled & Modified Release
18 Thickeners and Stabilizers
14 Disintegrants & Superdisintegrants
11 Lubricants & Glidants
9 Granulation
9 Direct Compression
8 Topical
7 Co-Processed Excipients
6 Film Formers & Plasticizers
5 Empty Capsules
5 API Stability Enhancers
5 Taste Masking
5 Solubilizers
4 Chewable & Orodispersible Aids
4 Vegetarian Capsules
3 Emulsifying Agents
3 Rheology Modifiers
2 Coloring Agents
1 Parenteral

DIGITAL CONTENT

81 News #PharmaBuzz

81 News #PharmaBuzz

GLOBAL SALES INFORMATION

25 US Medicaid Prescriptions, 336 Regulatory FDF Prices, 11 Annual Reports

25 US Medicaid Prescriptions
336 Regulatory FDF Prices
11 Annual Reports

MARKET PLACE

108 APIs, 44 FDF Dossiers

108 APIs
44 FDF Dossiers

PATENTS & EXCLUSIVITIES

14 US Patents, 6 US Exclusivities, 2 Health Canada Patents

14 US Patents
6 US Exclusivities
2 Health Canada Patents

REF. STANDARDS & IMPURITIES

3 EDQM, 2 USP, 30 Others

3 EDQM
2 USP
30 Others

ANALYTICAL

3 Analytical Methods

3 Analytical Methods

$ API Ref.Price (USD/KG) : 31 Xls

Filters

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Filters

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filter Applicant Reset all filters

114 All

01 1AA PHARMA INC

02 6ANGITA PHARMA INC.

03 10APOTEX INC

04 10AURO PHARMA INC

05 1BIO AGRI MIX LP

06 8GLAXOSMITHKLINE INC

07 1HUVEPHARMA EOOD

08 1INTERVET CANADA CORP

09 16JAMP PHARMA CORPORATION

10 4MANTRA PHARMA INC

11 2PHARMARIS CANADA INC

12 6PRO DOC LIMITEE

13 4Pharmascience Inc.

14 8SANDOZ CANADA INCORPORATED

15 8SANIS HEALTH INC

16 2SIVEM PHARMACEUTICALS ULC

17 5TEVA CANADA LIMITED

18 10VETOQUINOL N A INC

19 11ZOETIS CANADA INC

filter Active Ingredients Reset all filters

114 All

01 1AMOXICILLIN

02 67AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

03 3AMOXICILLIN TRIHYDRATE

04 4Amoxicillin Trihydrate

05 35CLAVULANIC ACID (CLAVULANATE POTASSIUM)

06 4CLAVULANIC ACID (POTASSIUM CLAVULANATE)

filter Dosage Form Reset all filters

114 All

01 18CAPSULE

02 5GRANULES FOR SUSPENSION

03 1POWDER

04 5POWDER FOR SOLUTION

05 31POWDER FOR SUSPENSION

06 35TABLET

07 19TABLET (CHEWABLE)

filter Brand Name Reset all filters

114 All

01 1AA-LANSOPRAZOLE-AMOXICILLIN-CLARITHROMYCIN

02 4AG-AMOXI CLAV

03 2AG-AMOXICILLIN

04 4AMOXICILLIN

05 2AMOXICILLIN CAPSULES BP

06 3AMOXICILLIN SODIUM AND POTASSIUM CLAVULANATE FOR INJECTION

07 1AMOXICILLIN SP

08 4AMOXICILLIN/CLAV

09 1AMOXIL

10 4APO-AMOXI

11 6APO-AMOXI CLAV

12 4AURO-AMOXICILLIN

13 6AURO-AMOXICLAV

14 8CLAVAMOX

15 2CLAVAMOX DROPS

16 2CLAVASEPTIN 250 MG

17 2CLAVASEPTIN 50 MG

18 2CLAVASEPTIN 500 MG

19 2CLAVASEPTIN 62.5MG

20 2CLAVASEPTIN 750 MG

21 2CLAVULIN 125 F ORAL SUS

22 2CLAVULIN 200

23 2CLAVULIN 250 F ORAL SUS

24 2CLAVULIN 400

25 1HUVAMOX

26 6JAMP AMOXI CLAV

27 6JAMP AMOXI CLAV SUSPENSION

28 4JAMP-AMOXICILLIN

29 4M-AMOXI CLAV

30 5NOVAMOXIN

31 1PARACILLIN SP

32 4PMS-AMOXICILLIN

33 1PRO-AMOX-250

34 1PRO-AMOX-500

35 4PRO-AMOXI CLAV

36 2PRZ-AMOXICILLIN

37 4SANDOZ AMOXI-CLAV TABLET

38 1SANDOZ AMOXICILLIN

List of Suppliers

Product Main Page

01

AA PHARMA INC

ASPEN

Not Confirmed

AA PHARMA INC

ASPEN

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN

Brand Name : AA-LANSOPRAZOLE-AMOXICILLIN-CLARITHROMYCIN

Dosage Form : CAPSULE

Dosage Strength : 500MG/CAP

Packaging :

Approval Date :

Application Number : 2470780

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

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Corporate PDF

02

ANGITA PHARMA INC.

ASPEN

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ANGITA PHARMA INC.

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : AG-AMOXICILLIN

Dosage Form : CAPSULE

Dosage Strength : 500MG

Packaging : 100/500

Approval Date :

Application Number : 2477726

Regulatory Info : Prescription

Registration Country : Canada

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Product Web Link

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03

ANGITA PHARMA INC.

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ANGITA PHARMA INC.

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : AG-AMOXI CLAV

Dosage Form : TABLET

Dosage Strength : 500MG

Packaging :

Approval Date :

Application Number : 2510634

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

ANGITA PHARMA INC.

ASPEN

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ANGITA PHARMA INC.

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Regulatory Info : Prescription

Registration Country : Canada

CLAVULANIC ACID (CLAVULANATE POTASSIUM)

Brand Name : AG-AMOXI CLAV

Dosage Form : TABLET

Dosage Strength : 125MG

Packaging :

Approval Date :

Application Number : 2510634

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

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05

ANGITA PHARMA INC.

ASPEN

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ANGITA PHARMA INC.

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : AG-AMOXI CLAV

Dosage Form : TABLET

Dosage Strength : 875MG

Packaging :

Approval Date :

Application Number : 2510642

Regulatory Info : Prescription

Registration Country : Canada

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Corporate PDF

06

ANGITA PHARMA INC.

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ANGITA PHARMA INC.

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Regulatory Info : Prescription

Registration Country : Canada

CLAVULANIC ACID (CLAVULANATE POTASSIUM)

Brand Name : AG-AMOXI CLAV

Dosage Form : TABLET

Dosage Strength : 125MG

Packaging :

Approval Date :

Application Number : 2510642

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

ANGITA PHARMA INC.

ASPEN

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ANGITA PHARMA INC.

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : AG-AMOXICILLIN

Dosage Form : POWDER FOR SUSPENSION

Dosage Strength : 250MG/5ML

Packaging :

Approval Date :

Application Number : 2537451

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

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08

APOTEX INC

ASPEN

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APOTEX INC

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : APO-AMOXI

Dosage Form : CAPSULE

Dosage Strength : 250MG

Packaging : 100/1000

Approval Date :

Application Number : 628115

Regulatory Info : Prescription

Registration Country : Canada

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09

APOTEX INC

ASPEN

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APOTEX INC

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : APO-AMOXI

Dosage Form : CAPSULE

Dosage Strength : 500MG

Packaging : 100/500

Approval Date :

Application Number : 628123

Regulatory Info : Prescription

Registration Country : Canada

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10

APOTEX INC

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APOTEX INC

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Regulatory Info : Prescription

Registration Country : Canada

AMOXICILLIN (AMOXICILLIN TRIHYDRATE)

Brand Name : APO-AMOXI

Dosage Form : POWDER FOR SUSPENSION

Dosage Strength : 125MG/5ML

Packaging :

Approval Date :

Application Number : 628131

Regulatory Info : Prescription

Registration Country : Canada

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Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.