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Fentanyl Citrate
Canada

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pharmacompass-2-m-2025-11-03

Fentanyl Citrate

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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

39 API Suppliers, 13 USDMF, 12 CEP/COS, 4 JDMF, 2 EU WC, 4 KDMF, 15 NDC API, 16 Listed Suppliers, $ API Reference Price

39 API Suppliers
13 USDMF
12 CEP/COS
4 JDMF
2 EU WC
4 KDMF
15 NDC API
16 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

7 Drugs in Development

7 Drugs in Development

FINISHED DOSAGE FORMULATIONS

495 FDF Dossiers, 77 FDA Orange Book, 374 Europe, 13 Canada, 3 South Africa, 28 Listed Dossiers

495 FDF Dossiers
77 FDA Orange Book
374 Europe
13 Canada
3 South Africa
28 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BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;BUCCAL, SUBLINGUAL - EQ 0.4MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.6MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.8MG BASE, TABLET;SUBLINGUAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, SPRAY, METERED;NASAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for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, 18 SPI Pharma, 2 DKSH, 2 Boai NKY Pharmaceuticals Ltd, 6 Gangwal Healthcare, 1 Nanjing Well Pharmaceutical, 2 Pfanstiehl, 5 Kirsch Pharma, 1 ACG Worldwide, 6 Actylis, 1 Alcedo Pharmachem, 7 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 4 BASF, 1 CD Formulation, 10 Corel Pharma Chem, 4 DFE Pharma, 1 Finar, 5 Gangwal Chemicals, 1 Huzhou Sunflower Pharmaceutical, 4 Ideal Cures, 5 Ingredion Pharma Solutions, 11 Kerry, 3 Keval Exports, 3 Kima Chemical, 6 Lonza Capsugel, 11 Microlex e.U, 2 Nitika Pharmaceutical Specialities, 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, 4 Silverline Chemicals, 2 The Dow Chemical Company, 1 Valens Pharmachem, 4 Vasa Pharmachem

EXCIPIENTS BY APPLICATIONS

55 Fillers, Diluents & Binders, 38 Coating Systems & Additives, 30 Disintegrants & Superdisintegrants, 27 Direct Compression, 21 Thickeners and Stabilizers, 19 Taste Masking, 18 Chewable & Orodispersible Aids, 17 Controlled & Modified Release, 16 Granulation, 13 Parenteral, 12 Co-Processed Excipients, 10 Lubricants & Glidants, 9 Film Formers & Plasticizers, 6 Solubilizers, 5 Empty Capsules, 5 Rheology Modifiers, 4 Vegetarian Capsules, 4 API Stability Enhancers, 3 Emulsifying Agents, 3 Topical, 2 Coloring Agents

55 Fillers, Diluents & Binders
38 Coating Systems & Additives
30 Disintegrants & Superdisintegrants
27 Direct Compression
21 Thickeners and Stabilizers
19 Taste Masking
18 Chewable & Orodispersible Aids
17 Controlled & Modified Release
16 Granulation
13 Parenteral
12 Co-Processed Excipients
10 Lubricants & Glidants
9 Film Formers & Plasticizers
6 Solubilizers
5 Empty Capsules
5 Rheology Modifiers
4 Vegetarian Capsules
4 API Stability Enhancers
3 Emulsifying Agents
3 Topical
2 Coloring Agents

DIGITAL CONTENT

1 Data Compilation #PharmaFlow, 36 News #PharmaBuzz

1 Data Compilation #PharmaFlow
36 News #PharmaBuzz

GLOBAL SALES INFORMATION

6 US Medicaid Prescriptions, 34 Regulatory FDF Prices, 8 Annual Reports

6 US Medicaid Prescriptions
34 Regulatory FDF Prices
8 Annual Reports

MARKET PLACE

13 APIs, 5 FDF Dossiers

13 APIs
5 FDF Dossiers

PATENTS & EXCLUSIVITIES

18 US Patents, 17 Health Canada Patents

18 US Patents
17 Health Canada Patents

REF. STANDARDS & IMPURITIES

2 EDQM, 3 Others

2 EDQM
3 Others

$ API Ref.Price (USD/KG) : 28,748 Xls

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13 All

01 1FRESENIUS KABI CANADA LTD

02 1JAMP PHARMA CORPORATION

03 2SANDOZ CANADA INCORPORATED

04 4STERIMAX INC

05 5TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

13 All

01 13FENTANYL (FENTANYL CITRATE)

filter Dosage Form Reset all filters

13 All

01 8SOLUTION

02 5TABLET (EFFERVESCENT)

filter Brand Name Reset all filters

13 All

01 1FENTANYL CITRATE INJECTION

02 1FENTANYL CITRATE INJECTION SDZ

03 1FENTANYL CITRATE INJECTION USP

04 1FENTANYL CITRATE INJECTION, USP

05 4FENTANYL INJECTION BP

06 5FENTORA

Aspen Fentanyl Citrate

List of Suppliers

Product Main Page

01

SANDOZ CANADA INCORPORATED

BioFit

Not Confirmed

SANDOZ CANADA INCORPORATED

BioFit

Not Confirmed

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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Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

SANDOZ CANADA INCORPORATED

BioFit

Not Confirmed

SANDOZ CANADA INCORPORATED

BioFit

Not Confirmed

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Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

03

STERIMAX INC

BioFit

Not Confirmed

STERIMAX INC

BioFit

Not Confirmed

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Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

STERIMAX INC

BioFit

Not Confirmed

STERIMAX INC

BioFit

Not Confirmed

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Digital Content

Regulatory Info : NARCOTICS (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL INJECTION BP

Dosage Form : SOLUTION

Dosage Strength : 250MCG/5ML

Packaging :

Approval Date :

Application Number : 2496151

Regulatory Info : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

05

STERIMAX INC

BioFit

Not Confirmed

STERIMAX INC

BioFit

Not Confirmed

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Regulatory Info : NARCOTICS (CDSA I)

Registration Country : Canada

FENTANYL (FENTANYL CITRATE)

Brand Name : FENTANYL INJECTION BP

Dosage Form : SOLUTION

Dosage Strength : 1000MCG/20ML

Packaging :

Approval Date :

Application Number : 2496178

Regulatory Info : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

06

TEVA CANADA LIMITED

BioFit

Not Confirmed

TEVA CANADA LIMITED

BioFit

Not Confirmed

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Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

TEVA CANADA LIMITED

BioFit

Not Confirmed

TEVA CANADA LIMITED

BioFit

Not Confirmed

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Digital Content

Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

08

TEVA CANADA LIMITED

BioFit

Not Confirmed

TEVA CANADA LIMITED

BioFit

Not Confirmed

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Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

09

TEVA CANADA LIMITED

BioFit

Not Confirmed

TEVA CANADA LIMITED

BioFit

Not Confirmed

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 : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

10

TEVA CANADA LIMITED

BioFit

Not Confirmed

TEVA CANADA LIMITED

BioFit

Not Confirmed

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Regulatory Info : NARCOTICS (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 : NARCOTICS (CDSA I)

Registration Country : Canada

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Product Web Link

Digital Content

Corporate PDF

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