FOSAMAX PLUS D | Health Canada | Drug Product Database | DPD | PharmaCompass.com

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FOSAMAX PLUS D
Canada

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Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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HealthTech BioActives, leading globally in Flavonoids and Vitamin B12 Derivatives.

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FOSAMAX PLUS D

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

56 API Suppliers, 24 USDMF, 13 CEP/COS, 6 JDMF, 10 EU WC, 4 KDMF, 11 NDC API, 21 Listed Suppliers, $ API Reference Price

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

DEVELOPMENTS

21 Drugs in Development

21 Drugs in Development

FINISHED DOSAGE FORMULATIONS

259 FDF Dossiers, 64 FDA Orange Book, 133 Europe, 23 Canada, 8 Australia, 3 South Africa, 28 Listed Dossiers

259 FDF Dossiers
64 FDA Orange Book
133 Europe
23 Canada
8 Australia
3 South Africa
28 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TABLET;ORAL - EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 70MG BASE, TABLET;ORAL - EQ 70MG BASE;2,800 IU, TABLET;ORAL - EQ 70MG BASE;5,600 IU

TABLET;ORAL - EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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, 18 SPI Pharma, 6 DKSH, 1 Pharm-RX Chemical, 3 Boai NKY Pharmaceuticals Ltd, 8 Gangwal Healthcare, 1 Nanjing Well Pharmaceutical, 2 Pfanstiehl, 3 Kirsch Pharma, 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, 5 Ingredion Pharma Solutions, 15 Kerry, 3 Keval Exports, 3 Lonza Capsugel, 12 Microlex e.U, 2 Nitika Pharmaceutical Specialities, 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, 10 Sigachi Industries, 4 Silverline Chemicals, 1 Ulanqab Kema New Material, 4 Vasa Pharmachem

EXCIPIENTS BY APPLICATIONS

60 Fillers, Diluents & Binders, 33 Direct Compression, 29 Disintegrants & Superdisintegrants, 24 Granulation, 24 Taste Masking, 19 Thickeners and Stabilizers, 17 Chewable & Orodispersible Aids, 14 Lubricants & Glidants, 14 Co-Processed Excipients, 8 Parenteral, 8 Empty Capsules, 6 Coating Systems & Additives, 4 Controlled & Modified Release, 3 API Stability Enhancers, 3 Solubilizers, 3 Emulsifying Agents, 2 Topical, 2 Rheology Modifiers, 1 Film Formers & Plasticizers, 1 Surfactant & Foaming Agents

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

DIGITAL CONTENT

1 Data Compilation #PharmaFlow, 25 News #PharmaBuzz

1 Data Compilation #PharmaFlow
25 News #PharmaBuzz

GLOBAL SALES INFORMATION

13 US Medicaid Prescriptions, 77 Regulatory FDF Prices

13 US Medicaid Prescriptions
77 Regulatory FDF Prices

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, 4 JP, 2 Others

2 EDQM
4 JP
2 Others

ANALYTICAL

1 BioAnalytical Methods

1 BioAnalytical Methods

$ API Ref.Price (USD/KG) : 218 Xls

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23 All

01 3ACCORD HEALTHCARE INC

02 1ANGITA PHARMA INC.

03 3APOTEX INC

04 2AURO PHARMA INC

05 1JAMP 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

23 All

01 21ALENDRONIC ACID (ALENDRONATE SODIUM)

02 2Alendronate Sodium

filter Dosage Form Reset all filters

23 All

01 23TABLET

filter Brand Name Reset all filters

23 All

01 3ACH-ALENDRONATE

02 1AG-ALENDRONATE SODIUM

03 2ALENDRONATE

04 1ALENDRONATE-70

05 1APO-ALENDRONATE

06 2APO-ALENDRONATE/VITAMIN D3

07 2AURO-ALENDRONATE

08 1FOSAMAX

09 1JAMP ALENDRONATE SODIUM

10 1M-ALENDRONATE

11 1MINT-ALENDRONATE

12 1NRA-ALENDRONATE

13 1PMS-ALENDRONATE

14 2PMS-ALENDRONATE-FC

15 1RIVA-ALENDRONATE FC

16 1SANDOZ ALENDRONATE

17 1TEVA-ALENDRONATE

Alendronate Sodium

List of Suppliers

Product Main Page

01

APOTEX INC

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Not Confirmed

APOTEX INC

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Digital Content

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

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02

Pharmascience Inc.

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Pharmascience Inc.

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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

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03

Pharmascience Inc.

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Pharmascience Inc.

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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

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04

PHARMASCIENCE INC

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PHARMASCIENCE INC

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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

Corporate PDF

05

PRO DOC LIMITEE

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PRO DOC LIMITEE

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

ALENDRONIC ACID (ALENDRONATE SODIUM)

Brand Name : ALENDRONATE-70

Dosage Form : TABLET

Dosage Strength : 70MG

Packaging : 4/100

Approval Date :

Application Number : 2303078

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

06

SANDOZ CANADA INCORPORATED

PREP

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SANDOZ CANADA INCORPORATED

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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

Portfolio PDF

Product Web Link

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Corporate PDF

07

SIVEM PHARMACEUTICALS ULC

PREP

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SIVEM PHARMACEUTICALS ULC

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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

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08

TEVA CANADA LIMITED

PREP

Not Confirmed

TEVA CANADA LIMITED

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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

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Corporate PDF

09

ORGANON CANADA INC.

Country

PREP

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ORGANON CANADA INC.

Country

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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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Website

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10

LABORATOIRE RIVA INC.

Country

PREP

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LABORATOIRE RIVA INC.

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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