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Fentanyl Citrate
Canada

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Veranova Fentanyl Citrate

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Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.

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Fentanyl Citrate

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ACTIVE PHARMA INGREDIENTS

31 API Suppliers, 14 USDMF, 12 CEP/COS, 4 JDMF, 3 EU WC, 4 KDMF, 15 NDC API, 16 Listed Suppliers, $ API Reference Price

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

FINISHED DOSAGE FORMULATIONS

381 FDF Dossiers, 77 FDA Orange Book, 159 Europe, 24 Canada, 75 Australia, 20 South Africa, 26 Listed Dossiers

381 FDF Dossiers
77 FDA Orange Book
159 Europe
24 Canada
75 Australia
20 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BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;BUCCAL, SUBLINGUAL - EQ 0.4MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.6MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.8MG BASE, TABLET;SUBLINGUAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for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, 18 SPI Pharma, 2 DKSH, 4 Faran Shimi Pharmaceutical, 2 Boai NKY Pharmaceuticals Ltd, 6 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

55 Fillers, Diluents & Binders, 42 Coating Systems & Additives, 30 Disintegrants & Superdisintegrants, 27 Direct Compression, 22 Controlled & Modified Release, 19 Thickeners and Stabilizers, 18 Taste Masking, 16 Granulation, 16 Chewable & Orodispersible Aids, 13 Co-Processed Excipients, 10 Lubricants & Glidants, 10 Film Formers & Plasticizers, 9 Parenteral, 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
42 Coating Systems & Additives
30 Disintegrants & Superdisintegrants
27 Direct Compression
22 Controlled & Modified Release
19 Thickeners and Stabilizers
18 Taste Masking
16 Granulation
16 Chewable & Orodispersible Aids
13 Co-Processed Excipients
10 Lubricants & Glidants
10 Film Formers & Plasticizers
9 Parenteral
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

2 US Medicaid Prescriptions, 103 Regulatory FDF Prices

2 US Medicaid Prescriptions
103 Regulatory FDF Prices

MARKET PLACE

12 APIs, 5 FDF Dossiers

12 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, 1 USP, 3 Others

2 EDQM
1 USP
3 Others

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

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24 All

01 1FRESENIUS KABI CANADA LTD

02 1JAMP PHARMA CORPORATION

03 8SANDOZ CANADA INCORPORATED

04 4STERIMAX INC

05 10TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

24 All

01 11FENTANYL

02 13FENTANYL (FENTANYL CITRATE)

filter Dosage Form Reset all filters

24 All

01 11PATCH

02 8SOLUTION

03 5TABLET (EFFERVESCENT)

filter Brand Name Reset all filters

24 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

07 6SANDOZ FENTANYL PATCH

08 5TEVA-FENTANYL

Aspen Fentanyl Citrate

List of Suppliers

Product Main Page

01

JAMP PHARMA CORPORATION

BePharma

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JAMP PHARMA CORPORATION

BePharma

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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

02

SANDOZ CANADA INCORPORATED

BePharma

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SANDOZ CANADA INCORPORATED

BePharma

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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

03

SANDOZ CANADA INCORPORATED

BePharma

Not Confirmed

SANDOZ CANADA INCORPORATED

BePharma

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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

04

SANDOZ CANADA INCORPORATED

BePharma

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SANDOZ CANADA INCORPORATED

BePharma

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 12MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327112

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

05

SANDOZ CANADA INCORPORATED

BePharma

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SANDOZ CANADA INCORPORATED

BePharma

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 25MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327120

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

06

SANDOZ CANADA INCORPORATED

BePharma

Not Confirmed

SANDOZ CANADA INCORPORATED

BePharma

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 37MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327139

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

07

SANDOZ CANADA INCORPORATED

BePharma

Not Confirmed

SANDOZ CANADA INCORPORATED

BePharma

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 50MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327147

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

08

SANDOZ CANADA INCORPORATED

BePharma

Not Confirmed

SANDOZ CANADA INCORPORATED

BePharma

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 75MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327155

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Product Web Link

Digital Content

09

TEVA CANADA LIMITED

BePharma

Not Confirmed

TEVA CANADA LIMITED

BePharma

Not Confirmed

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Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Brand Name : TEVA-FENTANYL

Dosage Form : PATCH

Dosage Strength : 12MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2311925

Regulatory Info : Narcotic (CDSA I)

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

10

TEVA CANADA LIMITED

BePharma

Not Confirmed

TEVA CANADA LIMITED

BePharma

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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

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