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Fentanyl Citrate
Canada

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Veranova Fentanyl Citrate

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Fentanyl Citrate

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CHEMISTRY
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ACTIVE PHARMA INGREDIENTS

32 API Suppliers, 14 USDMF, 12 CEP/COS, 3 JDMF, 3 EU WC, 4 KDMF, 16 NDC API, 17 Listed Suppliers, $ API Reference Price

32 API Suppliers
14 USDMF
12 CEP/COS
3 JDMF
3 EU WC
4 KDMF
16 NDC API
17 Listed Suppliers
$ API Reference Price

FINISHED DOSAGE FORMULATIONS

279 FDF Dossiers, 77 FDA Orange Book, 159 Europe, 14 Canada, 3 South Africa, 26 Listed Dossiers

279 FDF Dossiers
77 FDA Orange Book
159 Europe
14 Canada
3 South Africa
26 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.2MG BASE, TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.4MG BASE, TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.6MG BASE, TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.8MG BASE, TROCHE/LOZENGE;TRANSMUCOSAL - EQ 1.2MG BASE, TROCHE/LOZENGE;TRANSMUCOSAL - EQ 1.6MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.1MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.2MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;BUCCAL, SUBLINGUAL - EQ 0.4MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.6MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.8MG BASE, TABLET;SUBLINGUAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, SPRAY, METERED;NASAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, SPRAY, METERED;NASAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, SPRAY, METERED;NASAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.2MG BASE
TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.4MG BASE
TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.6MG BASE
TROCHE/LOZENGE;TRANSMUCOSAL - EQ 0.8MG BASE
TROCHE/LOZENGE;TRANSMUCOSAL - EQ 1.2MG BASE
TROCHE/LOZENGE;TRANSMUCOSAL - EQ 1.6MG BASE
TABLET;BUCCAL, SUBLINGUAL - EQ 0.1MG BASE
TABLET;BUCCAL, SUBLINGUAL - EQ 0.2MG BASE
TABLET;BUCCAL, SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;BUCCAL, SUBLINGUAL - EQ 0.4MG BASE
TABLET;BUCCAL, SUBLINGUAL - EQ 0.6MG BASE
TABLET;BUCCAL, SUBLINGUAL - EQ 0.8MG BASE
TABLET;SUBLINGUAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;SUBLINGUAL - EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;SUBLINGUAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;SUBLINGUAL - EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;SUBLINGUAL - EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
SPRAY, METERED;NASAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
SPRAY, METERED;NASAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
SPRAY, METERED;NASAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

RELATED EXCIPIENT COMPANIES

2 Rochem International Inc, 17 SPI Pharma, 1 Jai Radhe Sales, 2 Boai NKY Pharmaceuticals Ltd, 11 Gangwal Healthcare, 1 Nanjing Well Pharmaceutical, 2 Pfanstiehl, 1 ACG Worldwide, 6 Actylis, 1 Alcedo Pharmachem, 7 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 4 BASF, 10 Corel Pharma Chem, 4 DFE Pharma, 1 Finar, 5 Gangwal Chemicals, 1 Huzhou Sunflower Pharmaceutical, 5 Ideal Cures Pvt Ltd, 5 Ingredion Pharma Solutions, 17 Kerry, 3 Kima Chemical, 6 Lonza Capsugel, 11 Microlex e.U, 2 Novo Excipients, 2 Pharmatrans-Sanaq, 4 Pluviaendo, 4 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Qualicaps, 18 Roquette, 8 Seppic, 6 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 10 Sigachi Industries, 2 The Dow Chemical Company, 1 Valens Pharmachem, 4 Vasa Pharmachem

EXCIPIENTS BY APPLICATIONS

59 Fillers, Diluents & Binders, 42 Coating Systems & Additives, 34 Direct Compression, 28 Disintegrants & Superdisintegrants, 23 Controlled & Modified Release, 18 Thickeners and Stabilizers, 17 Taste Masking, 16 Granulation, 15 Chewable & Orodispersible Aids, 14 Co-Processed Excipients, 11 Lubricants & Glidants, 11 Film Formers & Plasticizers, 9 Parenteral, 5 Solubilizers, 5 Empty Capsules, 5 API Stability Enhancers, 4 Vegetarian Capsules, 3 Emulsifying Agents, 3 Topical, 3 Rheology Modifiers, 2 Coloring Agents

59 Fillers, Diluents & Binders
42 Coating Systems & Additives
34 Direct Compression
28 Disintegrants & Superdisintegrants
23 Controlled & Modified Release
18 Thickeners and Stabilizers
17 Taste Masking
16 Granulation
15 Chewable & Orodispersible Aids
14 Co-Processed Excipients
11 Lubricants & Glidants
11 Film Formers & Plasticizers
9 Parenteral
5 Solubilizers
5 Empty Capsules
5 API Stability Enhancers
4 Vegetarian Capsules
3 Emulsifying Agents
3 Topical
3 Rheology Modifiers
2 Coloring Agents

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow, 35 NEWS #PharmaBuzz

1 DATA COMPILATION #PharmaFlow
35 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

2 US Medicaid Prescriptions, 103 Finished Drug Prices

2 US Medicaid Prescriptions
103 Finished Drug Prices

MARKET PLACE

11 APIs, 5 FDF Dossiers

11 APIs
5 FDF Dossiers

PATENTS & EXCLUSIVITIES

36 US Patents, 17 Health Canada Patents

36 US Patents
17 Health Canada Patents

REF. STANDARDS & IMPURITIES

2 EDQM, 1 USP, 3 Others

2 EDQM
1 USP
3 Others

$ API Ref.Price (USD/KG) : 64,860 Xls

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14 All

01 1FRESENIUS KABI CANADA LTD

02 1HIKMA CANADA LIMITED

03 1JAMP PHARMA CORPORATION

04 2SANDOZ CANADA INCORPORATED

05 4STERIMAX INC

06 5TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

14 All

01 14FENTANYL (FENTANYL CITRATE)

filter Dosage Form Reset all filters

14 All

01 9SOLUTION

02 5TABLET (EFFERVESCENT)

filter Brand Name Reset all filters

14 All

01 1FENTANYL CITRATE INJECTION

02 1FENTANYL CITRATE INJECTION SDZ

03 2FENTANYL CITRATE INJECTION USP

04 1FENTANYL CITRATE INJECTION, USP

05 4FENTANYL INJECTION BP

06 5FENTORA

Aspen Fentanyl Citrate

List of Suppliers

Product Main Page

01

HIKMA CANADA LIMITED

PackExpo

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HIKMA CANADA LIMITED

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL CITRATE INJECTION USP

Dosage Form : SOLUTION

Dosage Strength : 50MCG/ML

Packaging : 2ML/10ML

Approval Date :

Application Number : 2385406

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

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02

JAMP PHARMA CORPORATION

PackExpo

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JAMP PHARMA CORPORATION

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL CITRATE INJECTION

Dosage Form : SOLUTION

Dosage Strength : 50MCG/ML

Packaging :

Approval Date :

Application Number : 2506963

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

03

SANDOZ CANADA INCORPORATED

PackExpo

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SANDOZ CANADA INCORPORATED

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL CITRATE INJECTION USP

Dosage Form : SOLUTION

Dosage Strength : 50MCG/ML

Packaging : 2/5/10/20/50ML

Approval Date :

Application Number : 2240434

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

04

SANDOZ CANADA INCORPORATED

PackExpo

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SANDOZ CANADA INCORPORATED

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL CITRATE INJECTION SDZ

Dosage Form : SOLUTION

Dosage Strength : 50MCG/ML

Packaging : 10ML

Approval Date :

Application Number : 2384124

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

05

STERIMAX INC

PackExpo

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STERIMAX INC

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL INJECTION BP

Dosage Form : SOLUTION

Dosage Strength : 100MCG/2ML

Packaging :

Approval Date :

Application Number : 2496143

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

06

TEVA CANADA LIMITED

PackExpo

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TEVA CANADA LIMITED

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTORA

Dosage Form : TABLET (EFFERVESCENT)

Dosage Strength : 100MCG

Packaging : 28

Approval Date :

Application Number : 2408007

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

TEVA CANADA LIMITED

PackExpo

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TEVA CANADA LIMITED

PackExpo

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Digital Content

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTORA

Dosage Form : TABLET (EFFERVESCENT)

Dosage Strength : 200MCG

Packaging : 28

Approval Date :

Application Number : 2408015

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

08

TEVA CANADA LIMITED

PackExpo

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TEVA CANADA LIMITED

PackExpo

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Digital Content

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTORA

Dosage Form : TABLET (EFFERVESCENT)

Dosage Strength : 400MCG

Packaging : 28

Approval Date :

Application Number : 2408023

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

09

TEVA CANADA LIMITED

PackExpo

Not Confirmed

TEVA CANADA LIMITED

PackExpo

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Digital Content

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTORA

Dosage Form : TABLET (EFFERVESCENT)

Dosage Strength : 600MCG

Packaging : 28

Approval Date :

Application Number : 2408031

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

10

TEVA CANADA LIMITED

PackExpo

Not Confirmed

TEVA CANADA LIMITED

PackExpo

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTORA

Dosage Form : TABLET (EFFERVESCENT)

Dosage Strength : 800MCG

Packaging : 28

Approval Date :

Application Number : 2408058

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

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Product Web Link

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