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Fentanyl Citrate
Canada

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Veranova Fentanyl Citrate

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Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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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, 4 JDMF, 3 EU WC, 4 KDMF, 16 NDC API, 17 Listed Suppliers, $ API Reference Price

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

FINISHED DOSAGE FORMULATIONS

379 FDF Dossiers, 77 FDA Orange Book, 159 Europe, 25 Canada, 75 Australia, 17 South Africa, 26 Listed Dossiers

379 FDF Dossiers
77 FDA Orange Book
159 Europe
25 Canada
75 Australia
17 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BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;BUCCAL, SUBLINGUAL - EQ 0.4MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.6MG BASE, TABLET;BUCCAL, SUBLINGUAL - EQ 0.8MG BASE, TABLET;SUBLINGUAL - EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;SUBLINGUAL - EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for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, 4 Faran Shimi Pharmaceutical, 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, 15 Co-Processed Excipients, 11 Lubricants & Glidants, 11 Film Formers & Plasticizers, 9 Parenteral, 5 Empty Capsules, 5 API Stability Enhancers, 5 Solubilizers, 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
15 Co-Processed Excipients
11 Lubricants & Glidants
11 Film Formers & Plasticizers
9 Parenteral
5 Empty Capsules
5 API Stability Enhancers
5 Solubilizers
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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01 1FRESENIUS KABI CANADA LTD

02 1HIKMA CANADA LIMITED

03 1JAMP PHARMA CORPORATION

04 8SANDOZ CANADA INCORPORATED

05 4STERIMAX INC

06 10TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

25 All

01 11FENTANYL

02 14FENTANYL (FENTANYL CITRATE)

filter Dosage Form Reset all filters

25 All

01 11PATCH

02 9SOLUTION

03 5TABLET (EFFERVESCENT)

filter Brand Name Reset all filters

25 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

07 6SANDOZ FENTANYL PATCH

08 5TEVA-FENTANYL

Aspen Fentanyl Citrate

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Product Main Page

01

HIKMA CANADA LIMITED

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HIKMA CANADA LIMITED

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Regulatory Info :

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 :

Registration Country : Canada

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02

JAMP PHARMA CORPORATION

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JAMP PHARMA CORPORATION

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Regulatory Info :

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 :

Registration Country : Canada

Portfolio PDF

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03

SANDOZ CANADA INCORPORATED

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Regulatory Info :

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 :

Registration Country : Canada

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04

SANDOZ CANADA INCORPORATED

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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 :

Registration Country : Canada

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05

SANDOZ CANADA INCORPORATED

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Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 12MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327112

Regulatory Info :

Registration Country : Canada

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06

SANDOZ CANADA INCORPORATED

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Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 25MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327120

Regulatory Info :

Registration Country : Canada

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07

SANDOZ CANADA INCORPORATED

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Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 37MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327139

Regulatory Info :

Registration Country : Canada

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SANDOZ CANADA INCORPORATED

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Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 50MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327147

Regulatory Info :

Registration Country : Canada

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SANDOZ CANADA INCORPORATED

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Regulatory Info :

Registration Country : Canada

Brand Name : SANDOZ FENTANYL PATCH

Dosage Form : PATCH

Dosage Strength : 75MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2327155

Regulatory Info :

Registration Country : Canada

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10

TEVA CANADA LIMITED

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TEVA CANADA LIMITED

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Regulatory Info :

Registration Country : Canada

Brand Name : TEVA-FENTANYL

Dosage Form : PATCH

Dosage Strength : 12MCG/HOUR

Packaging : 5

Approval Date :

Application Number : 2311925

Regulatory Info :

Registration Country : Canada

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