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Ropinirole Hydrochloride
Listed Dossiers

With Fermion, start the journey of your innovative API.

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Suanfarma CDMO offers integrated end-to-end solutions for development & commercialization of intermediates & APIs for small molecules.

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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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Ropinirole Hydrochloride

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ACTIVE PHARMA INGREDIENTS

25 API Suppliers, 11 USDMF, 5 CEP/COS, 4 JDMF, 7 EU WC, 5 KDMF, 9 NDC API, 11 Listed Suppliers, $ API Reference Price

25 API Suppliers
11 USDMF
5 CEP/COS
4 JDMF
7 EU WC
5 KDMF
9 NDC API
11 Listed Suppliers
$ API Reference Price

INTERMEDIATES

3 Intermediate Suppliers

3 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

222 FDF Dossiers, 138 FDA Orange Book, 60 Europe, 12 Canada, 5 South Africa, 7 Listed Dossiers

222 FDF Dossiers
138 FDA Orange Book
60 Europe
12 Canada
5 South Africa
7 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - EQ 0.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET;ORAL - EQ 0.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - EQ 8MG 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, 8 DKSH, 6 Faran Shimi Pharmaceutical, 4 Boai NKY Pharmaceuticals Ltd, 5 Gangwal Healthcare, 8 Nanjing Well Pharmaceutical, 1 Pfanstiehl, 1 ACG Worldwide, 6 Actylis, 1 Aeon Procare, 7 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 2 Ashland, 23 BASF, 1 Clariant, 12 Corel Pharma Chem, 6 DFE Pharma, 1 Esteem Industries, 2 Finar, 11 Gangwal Chemicals, 5 Ideal Cures, 4 Ingredion Pharma Solutions, 39 Kerry, 5 Kima Chemical, 6 Lonza Capsugel, 17 Microlex e.U, 1 Nanjing Bold Chemical, 2 Nitika Pharmaceutical Specialities, 2 Nomisma Healthcare, 3 Novo Excipients, 2 Pharmatrans-Sanaq, 6 Pluviaendo, 3 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Qualicaps, 23 Roquette, 13 Seppic, 7 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shanghai Welltone Material Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 10 Sigachi Industries, 3 Silverline Chemicals, 4 The Dow Chemical Company, 1 Ulanqab Kema New Material, 1 Valens Pharmachem, 3 Vasa Pharmachem, 1 Vertellus

EXCIPIENTS BY APPLICATIONS

91 Fillers, Diluents & Binders, 53 Coating Systems & Additives, 34 Controlled & Modified Release, 33 Direct Compression, 31 Thickeners and Stabilizers, 31 Solubilizers, 27 Granulation, 24 Disintegrants & Superdisintegrants, 23 Co-Processed Excipients, 21 Taste Masking, 20 Film Formers & Plasticizers, 17 Parenteral, 17 Topical, 16 Chewable & Orodispersible Aids, 16 Lubricants & Glidants, 11 Rheology Modifiers, 10 Emulsifying Agents, 7 API Stability Enhancers, 5 Empty Capsules, 5 Coloring Agents, 4 Vegetarian Capsules, 4 Surfactant & Foaming Agents

91 Fillers, Diluents & Binders
53 Coating Systems & Additives
34 Controlled & Modified Release
33 Direct Compression
31 Thickeners and Stabilizers
31 Solubilizers
27 Granulation
24 Disintegrants & Superdisintegrants
23 Co-Processed Excipients
21 Taste Masking
20 Film Formers & Plasticizers
17 Parenteral
17 Topical
16 Chewable & Orodispersible Aids
16 Lubricants & Glidants
11 Rheology Modifiers
10 Emulsifying Agents
7 API Stability Enhancers
5 Empty Capsules
5 Coloring Agents
4 Vegetarian Capsules
4 Surfactant & Foaming Agents

DIGITAL CONTENT

1 News #PharmaBuzz

1 News #PharmaBuzz

GLOBAL SALES INFORMATION

1 US Medicaid Prescriptions, 53 Regulatory FDF Prices, 1 Annual Reports

1 US Medicaid Prescriptions
53 Regulatory FDF Prices
1 Annual Reports

MARKET PLACE

3 APIs

3 APIs

PATENTS & EXCLUSIVITIES

18 Health Canada Patents

18 Health Canada Patents

REF. STANDARDS & IMPURITIES

1 Others

1 Others

ANALYTICAL

1 BioAnalytical Methods

1 BioAnalytical Methods

$ API Ref.Price (USD/KG) : 4,775 Xls

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01 7Orchid Chemicals & Pharmaceuticals Ltd

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01 7Ropinirole Hydrochloride

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01 7TABLET

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01 10.25MG

02 10.5MG

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01 7India

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Orchid Chemicals & Pharmaceuticals Ltd

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Regulatory Info : Generic EU CTD

Registration Country : India

Ropinirole Hydrochloride

Brand Name :

Dosage Form : TABLET

Dosage Strength : 0.25MG

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Approval Date :

Application Number :

Regulatory Info : Generic EU CTD

Registration Country : India

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Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Orchid Chemicals & Pharmaceuticals Ltd

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Regulatory Info : Generic EU CTD

Ropinirole Hydrochloride

Dosage : TABLET

Dosage Strength : 0.25MG

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Registration Country : India

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Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Registration Country : India

Ropinirole Hydrochloride

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Dosage Strength : 0.5MG

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Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Ropinirole Hydrochloride

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Orchid Chemicals & Pharmaceuticals Ltd

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Orchid Chemicals & Pharmaceuticals Ltd

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Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Orchid Chemicals & Pharmaceuticals Ltd

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Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Regulatory Info : Generic EU CTD

Registration Country : India

Ropinirole Hydrochloride

Brand Name :

Dosage Form : TABLET

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Generic EU CTD

Registration Country : India

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Product Web Link

Digital Content

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07

Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

Not Confirmed

Orchid Chemicals & Pharmaceuticals Ltd

Indo Livestock Expo

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Packaging :

Regulatory Info : Generic EU CTD

Ropinirole Hydrochloride

Dosage : TABLET

Dosage Strength : 5MG

Brand Name :

Approval Date :

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Registration Country : India

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