Degarelix Acetate | FDA Orange Book | Approved Drug Product List | PharmaCompass.com

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Degarelix Acetate
FDA Orange Book

Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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Jai Radhe Sales is your partner for all your sourcing needs.

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Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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Degarelix Acetate

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

17 API Suppliers, 8 USDMF, 1 KDMF, 15 NDC API, 11 Listed Suppliers, $ API Reference Price

17 API Suppliers
8 USDMF
1 KDMF
15 NDC API
11 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

1 Drugs in Development

1 Drugs in Development

FINISHED DOSAGE FORMULATIONS

18 FDF Dossiers, 2 FDA Orange Book, 8 Europe, 2 Canada, 2 Australia, 2 South Africa, 2 Listed Dossiers

18 FDF Dossiers
2 FDA Orange Book
8 Europe
2 Canada
2 Australia
2 South Africa
2 Listed Dossiers

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow, 8 NEWS #PharmaBuzz

1 DATA COMPILATION #PharmaFlow
8 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

1 US Medicaid Prescriptions, 6 Finished Drug Prices, 7 Annual Reports

1 US Medicaid Prescriptions
6 Finished Drug Prices
7 Annual Reports

MARKET PLACE

1 APIs, 1 FDF Dossiers

1 APIs
1 FDF Dossiers

PATENTS & EXCLUSIVITIES

14 US Patents, 2 Health Canada Patents

14 US Patents
2 Health Canada Patents

REF. STANDARDS & IMPURITIES

1 Others

1 Others

$ API Ref.Price (USD/KG) : 291,617 Xls

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01 2FERRING

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01 2POWDER;SUBCUTANEOUS

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01 2RX

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01 2FIRMAGON

filter RLD Reset all filters

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01 2Yes

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RLD : Yes

TE Code :

DEGARELIX ACETATE

Brand Name : FIRMAGON

Dosage Form : POWDER;SUBCUTANEOUS

Dosage Strength : EQ 80MG BASE/VIAL

Approval Date : 2008-12-24

Application Number : 22201

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Portfolio PDF

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Digital Content

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02

FERRING

Pharmtech & Ingredients

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FERRING

Pharmtech & Ingredients

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RLD : Yes

TE Code :

DEGARELIX ACETATE

Brand Name : FIRMAGON

Dosage Form : POWDER;SUBCUTANEOUS

Dosage Strength : EQ 120MG BASE/VIAL

Approval Date : 2008-12-24

Application Number : 22201

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

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