Bupropion hydrochloride (JAN/USP) | Suppliers | Impurities | Impurity Standards| PharmaCompass.com

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Bupropion Hydrochloride (JAN/USP)
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Bupropion hydrochloride (JAN/USP)

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ACTIVE PHARMA INGREDIENTS

74 API Suppliers, 37 USDMF, 11 EU WC, 10 KDMF, 34 NDC API, 34 Listed Suppliers, $ API Reference Price

74 API Suppliers
37 USDMF
11 EU WC
10 KDMF
34 NDC API
34 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

32 Drugs in Development

32 Drugs in Development

INTERMEDIATES

6 Intermediate Suppliers

6 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

273 FDF Dossiers, 136 FDA Orange Book, 85 Europe, 12 Canada, 2 Australia, 19 South Africa, 19 Listed Dossiers

273 FDF Dossiers
136 FDA Orange Book
85 Europe
12 Canada
2 Australia
19 South Africa
19 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG, TABLET, EXTENDED RELEASE;ORAL - 100MG, TABLET, EXTENDED RELEASE;ORAL - 150MG, TABLET, EXTENDED RELEASE;ORAL - 200MG, TABLET, EXTENDED RELEASE;ORAL - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 150MG, TABLET, EXTENDED RELEASE;ORAL - 300MG, TABLET, EXTENDED RELEASE;ORAL - 450MG

TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG
TABLET, EXTENDED RELEASE;ORAL - 100MG
TABLET, EXTENDED RELEASE;ORAL - 150MG
TABLET, EXTENDED RELEASE;ORAL - 200MG
TABLET, EXTENDED RELEASE;ORAL - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 150MG
TABLET, EXTENDED RELEASE;ORAL - 300MG
TABLET, EXTENDED RELEASE;ORAL - 450MG

RELATED EXCIPIENT COMPANIES

1 Minakem, 7 Evonik, 2 Rochem International Inc, 20 SPI Pharma, 17 DKSH, 7 Faran Shimi Pharmaceutical, 3 Boai NKY Pharmaceuticals Ltd, 5 Gangwal Healthcare, 9 Nanjing Well Pharmaceutical, 1 Shanghai Minbiotech, 1 Pfanstiehl, 1 Capital Farma, 1 ACG Worldwide, 6 Actylis, 1 Aeon Procare, 2 Alcedo Pharmachem, 6 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 3 Ashland, 35 BASF, 2 Clariant, 16 Corel Pharma Chem, 5 DFE Pharma, 3 Doshion Polyscience, 1 Esteem Industries, 3 Finar, 12 Gangwal Chemicals, 1 Huzhou Sunflower Pharmaceutical, 13 Ideal Cures, 3 Ingredion Pharma Solutions, 39 Kerry, 2 Keval Exports, 5 Kima Chemical, 6 Lonza Capsugel, 21 Microlex e.U, 1 Nanjing Bold Chemical, 3 Nitika Pharmaceutical Specialities, 2 Nomisma Healthcare, 4 Novo Excipients, 3 Pharmatrans-Sanaq, 7 Pluviaendo, 2 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Qualicaps, 19 Roquette, 14 Seppic, 5 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 9 Sigachi Industries, 2 Silverline Chemicals, 4 The Dow Chemical Company, 2 Valens Pharmachem, 2 Vasa Pharmachem, 2 Vertellus

EXCIPIENTS BY APPLICATIONS

100 Fillers, Diluents & Binders, 79 Coating Systems & Additives, 50 Controlled & Modified Release, 40 Solubilizers, 37 Direct Compression, 33 Thickeners and Stabilizers, 30 Granulation, 29 Lubricants & Glidants, 28 Film Formers & Plasticizers, 28 Taste Masking, 23 Topical, 21 Co-Processed Excipients, 20 Parenteral, 17 Disintegrants & Superdisintegrants, 17 Chewable & Orodispersible Aids, 10 Emulsifying Agents, 10 Rheology Modifiers, 7 API Stability Enhancers, 5 Empty Capsules, 5 Surfactant & Foaming Agents, 5 Coloring Agents, 4 Vegetarian Capsules

100 Fillers, Diluents & Binders
79 Coating Systems & Additives
50 Controlled & Modified Release
40 Solubilizers
37 Direct Compression
33 Thickeners and Stabilizers
30 Granulation
29 Lubricants & Glidants
28 Film Formers & Plasticizers
28 Taste Masking
23 Topical
21 Co-Processed Excipients
20 Parenteral
17 Disintegrants & Superdisintegrants
17 Chewable & Orodispersible Aids
10 Emulsifying Agents
10 Rheology Modifiers
7 API Stability Enhancers
5 Empty Capsules
5 Surfactant & Foaming Agents
5 Coloring Agents
4 Vegetarian Capsules

DIGITAL CONTENT

95 News #PharmaBuzz

95 News #PharmaBuzz

GLOBAL SALES INFORMATION

58 US Medicaid Prescriptions, 62 Regulatory FDF Prices, 10 Annual Reports

58 US Medicaid Prescriptions
62 Regulatory FDF Prices
10 Annual Reports

MARKET PLACE

12 APIs, 2 FDF Dossiers

12 APIs
2 FDF Dossiers

PATENTS & EXCLUSIVITIES

20 US Patents, 30 Health Canada Patents

20 US Patents
30 Health Canada Patents

REF. STANDARDS & IMPURITIES

4 USP, 16 Others

4 USP
16 Others

ANALYTICAL

2 BioAnalytical Methods

2 BioAnalytical Methods

$ API Ref.Price (USD/KG) : 63 Xls

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16 All

01 2 Aozeal Certified Standards

02 8Clearsynth

03 6USP

filter CAS Number Reset all filters

16 All

01 11049718-43-5

02 11049718-57-1

03 21049718-72-0

04 11193779-34-8

05 1119802-69-6(Freebase)

06 11346598-72-8

07 11346603-00-6

08 131677-93-7

09 234911-51-8

10 163199-74-6

11 2857233-13-7

12 2Blank

filter Details Reset all filters

16 All

01 1Cat No. CS-O-07425 // Impurity

02 1Cat No. CS-O-07426 // Impurity

03 1Cat No. CS-O-07427 // Impurity

04 1Cat No. CS-O-07436 // Impurity

05 1Cat No. CS-O-07437 // Impurity

06 1Cat No. CS-O-07439 // Impurity

07 1Cat No. CS-O-07441 // Impurity

08 1Cat No. CS-O-14091 // Impurity

09 2In stock

10 6Material Origin- Chemical Synthesis; USMCA- No; KORUS- No

filter Country Reset all filters

16 All

01 6Gabon

02 8India

03 2U.S.A

Product Main Page

01

Aozeal Certified Standards

Pharmex

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Aozeal Certified Standards

Pharmex

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Bupropion Impurity 11

CAS Number : 1346603-00-6

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Details : In stock

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Storage :

Code/Batch No : B0002.40

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Aozeal Certified Standards

Pharmex

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Aozeal Certified Standards

Pharmex

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Bupropion Impurity 3

CAS Number : 1346598-72-8

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Code/Batch No : B0002.32

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Clearsynth Labs Limited

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Clearsynth Labs Limited

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2-Bromo Bupropion Impurity

CAS Number : 34911-51-8

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Details : Cat No. CS-O-07425 // Impurity

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Clearsynth Labs Limited

Pharmex

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Bupropion 2-Chloro Isomer

CAS Number : 1049718-57-1

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Details : Cat No. CS-O-07426 // Impurity

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Clearsynth Labs Limited

Pharmex

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3,4-Dichloro Bupropion

CAS Number : 1193779-34-8

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Details : Cat No. CS-O-07427 // Impurity

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Clearsynth Labs Limited

Pharmex

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Bupropion USP Related Compound A

CAS Number : 1049718-72-0

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Details : Cat No. CS-O-07436 // Impurity

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Clearsynth Labs Limited

Pharmex

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Bupropion USP Related Compound B

CAS Number : 1049718-43-5

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Details : Cat No. CS-O-07437 // Impurity

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Clearsynth Labs Limited

Pharmex

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Bupropion USP Related Compound D

CAS Number : 63199-74-6

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Details : Cat No. CS-O-07439 // Impurity

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Clearsynth Labs Limited

Pharmex

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Clearsynth Labs Limited

Pharmex

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Bupropion USP Related Compound F

CAS Number : 857233-13-7

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Details : Cat No. CS-O-07441 // Impurity

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Code/Batch No :

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10

Clearsynth Labs Limited

Pharmex

Not Confirmed

Clearsynth Labs Limited

Pharmex

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Bupropion Amino Impurity

CAS Number : 119802-69-6(Freebase)

Quantity Per Vial :

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Details : Cat No. CS-O-14091 // Impurity

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