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Alendronate Sodium
Canada

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Alendronate Sodium

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

49 API Suppliers, 24 USDMF, 13 CEP/COS, 6 JDMF, 10 EU WC, 13 KDMF, 11 NDC API, 20 Listed Suppliers, $ API Reference Price

49 API Suppliers
24 USDMF
13 CEP/COS
6 JDMF
10 EU WC
13 KDMF
11 NDC API
20 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

2 Drugs in Development

2 Drugs in Development

FINISHED DOSAGE FORMULATIONS

232 FDF Dossiers, 64 FDA Orange Book, 107 Europe, 25 Canada, 6 Australia, 3 South Africa, 27 Listed Dossiers

232 FDF Dossiers
64 FDA Orange Book
107 Europe
25 Canada
6 Australia
3 South Africa
27 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 70MG BASE, TABLET;ORAL - EQ 70MG BASE;2,800 IU, TABLET;ORAL - EQ 70MG BASE;5,600 IU

TABLET;ORAL - EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 70MG BASE
TABLET;ORAL - EQ 70MG BASE;2,800 IU
TABLET;ORAL - EQ 70MG BASE;5,600 IU

RELATED EXCIPIENT COMPANIES

4 Rochem International Inc, 17 SPI Pharma, 6 DKSH, 1 Pharm-RX Chemical, 7 Faran Shimi Pharmaceutical, 3 Boai NKY Pharmaceuticals Ltd, 14 Gangwal Healthcare, 1 Nanjing Well Pharmaceutical, 2 Pfanstiehl, 4 ACG Worldwide, 2 Actylis, 7 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 7 BASF, 1 Bioplus Life Sciences, 7 DFE Pharma, 5 Gangwal Chemicals, 1 Ideal Cures Pvt Ltd, 5 Ingredion Pharma Solutions, 26 Kerry, 3 Lonza Capsugel, 12 Microlex e.U, 2 Pharmatrans-Sanaq, 7 Pluviaendo, 4 Prachin Chemical, 1 Qualicaps, 18 Roquette, 1 Seppic, 6 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shanghai Welltone Material Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 11 Sigachi Industries, 1 Ulanqab Kema New Material, 4 Vasa Pharmachem

EXCIPIENTS BY APPLICATIONS

79 Fillers, Diluents & Binders, 36 Direct Compression, 27 Disintegrants & Superdisintegrants, 23 Taste Masking, 20 Thickeners and Stabilizers, 20 Co-Processed Excipients, 19 Granulation, 15 Lubricants & Glidants, 14 Chewable & Orodispersible Aids, 8 Empty Capsules, 7 Coating Systems & Additives, 6 Controlled & Modified Release, 6 Parenteral, 4 API Stability Enhancers, 3 Emulsifying Agents, 2 Solubilizers, 2 Topical, 2 Rheology Modifiers, 1 Film Formers & Plasticizers, 1 Surfactant & Foaming Agents

79 Fillers, Diluents & Binders
36 Direct Compression
27 Disintegrants & Superdisintegrants
23 Taste Masking
20 Thickeners and Stabilizers
20 Co-Processed Excipients
19 Granulation
15 Lubricants & Glidants
14 Chewable & Orodispersible Aids
8 Empty Capsules
7 Coating Systems & Additives
6 Controlled & Modified Release
6 Parenteral
4 API Stability Enhancers
3 Emulsifying Agents
2 Solubilizers
2 Topical
2 Rheology Modifiers
1 Film Formers & Plasticizers
1 Surfactant & Foaming Agents

DIGITAL CONTENT

5 DATA COMPILATION #PharmaFlow, 25 NEWS #PharmaBuzz

5 DATA COMPILATION #PharmaFlow
25 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

4 US Medicaid Prescriptions, 120 Finished Drug Prices, 5 Annual Reports

4 US Medicaid Prescriptions
120 Finished Drug Prices
5 Annual Reports

MARKET PLACE

10 APIs, 1 FDF Dossiers

10 APIs
1 FDF Dossiers

PATENTS & EXCLUSIVITIES

1 US Patents, 17 Health Canada Patents

1 US Patents
17 Health Canada Patents

REF. STANDARDS & IMPURITIES

2 EDQM, 1 USP, 4 JP, 1 Others

2 EDQM
1 USP
4 JP
1 Others

ANALYTICAL

1 BioAnalytical Methods

1 BioAnalytical Methods

$ API Ref.Price (USD/KG) : 182 Xls

Filters

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25 All

01 3ACCORD HEALTHCARE INC

02 2ANGITA PHARMA INC.

03 3APOTEX INC

04 2AURO PHARMA INC

05 2JAMP PHARMA CORPORATION

06 1LABORATOIRE RIVA INC.

07 1MANTRA PHARMA INC

08 1MINT PHARMACEUTICALS INC

09 1NORA PHARMA INC

10 1ORGANON CANADA INC.

11 1PHARMASCIENCE INC

12 1PRO DOC LIMITEE

13 2Pharmascience Inc.

14 1SANDOZ CANADA INCORPORATED

15 1SANIS HEALTH INC

16 1SIVEM PHARMACEUTICALS ULC

17 1TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

25 All

01 23ALENDRONIC ACID (ALENDRONATE SODIUM)

02 2Alendronate Sodium

filter Dosage Form Reset all filters

25 All

01 25TABLET

filter Brand Name Reset all filters

25 All

01 3ACH-ALENDRONATE

02 1AG-ALENDRONATE

03 1AG-ALENDRONATE SODIUM

04 2ALENDRONATE

05 1ALENDRONATE-70

06 1APO-ALENDRONATE

07 2APO-ALENDRONATE/VITAMIN D3

08 2AURO-ALENDRONATE

09 1FOSAMAX

10 1JAMP ALENDRONATE SODIUM

11 1JAMP-ALENDRONATE

12 1M-ALENDRONATE

13 1MINT-ALENDRONATE

14 1NRA-ALENDRONATE

15 1PMS-ALENDRONATE

16 2PMS-ALENDRONATE-FC

17 1RIVA-ALENDRONATE FC

18 1SANDOZ ALENDRONATE

19 1TEVA-ALENDRONATE

Alendronate Sodium

List of Suppliers

Product Main Page

01

APOTEX INC

Antibody Engineering

Not Confirmed

APOTEX INC

Antibody Engineering

Not Confirmed

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : APO-ALENDRONATE

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 4

Approval Date :

Application Number : 2248730

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

JAMP PHARMA CORPORATION

Antibody Engineering

Not Confirmed

JAMP PHARMA CORPORATION

Antibody Engineering

Not Confirmed

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : JAMP-ALENDRONATE

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 4

Approval Date :

Application Number : 2385031

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

03

Pharmascience Inc.

Antibody Engineering

Not Confirmed

Pharmascience Inc.

Antibody Engineering

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

Alendronate Sodium

Brand Name : PMS-ALENDRONATE

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

04

Pharmascience Inc.

Antibody Engineering

Not Confirmed

Pharmascience Inc.

Antibody Engineering

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

Alendronate Sodium

Brand Name : PMS-ALENDRONATE-FC

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 30

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

05

PHARMASCIENCE INC

Antibody Engineering

Not Confirmed

PHARMASCIENCE INC

Antibody Engineering

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : PMS-ALENDRONATE-FC

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 30

Approval Date :

Application Number : 2284006

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

06

SANDOZ CANADA INCORPORATED

Antibody Engineering

Not Confirmed

SANDOZ CANADA INCORPORATED

Antibody Engineering

Not Confirmed

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : SANDOZ ALENDRONATE

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 4

Approval Date :

Application Number : 2288109

Regulatory Info : Prescription

Registration Country : Canada

Product Web Link

Digital Content

07

SIVEM PHARMACEUTICALS ULC

Antibody Engineering

Not Confirmed

SIVEM PHARMACEUTICALS ULC

Antibody Engineering

Not Confirmed

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : ALENDRONATE

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging :

Approval Date :

Application Number : 2299712

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

08

TEVA CANADA LIMITED

Antibody Engineering

Not Confirmed

TEVA CANADA LIMITED

Antibody Engineering

Not Confirmed

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : TEVA-ALENDRONATE

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 4

Approval Date :

Application Number : 2261715

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

09

ORGANON CANADA INC.

Country

Antibody Engineering

Not Confirmed

ORGANON CANADA INC.

Country

Antibody Engineering

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : FOSAMAX

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging :

Approval Date :

Application Number : 2245329

Regulatory Info : Prescription

Registration Country : Canada

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Virtual Booth

Digital Content

Website

Corporate PDF

10

LABORATOIRE RIVA INC.

Country

Antibody Engineering

Not Confirmed

LABORATOIRE RIVA INC.

Country

Antibody Engineering

Not Confirmed

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Country

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Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : RIVA-ALENDRONATE FC

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : Apr-50

Approval Date :

Application Number : 2270889

Regulatory Info : Prescription

Registration Country : Canada

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