Find Antihemophilic factor recombinant manufacturers, exporters & distributors on PharmaCompass

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Synopsis

Synopsis

ACTIVE PHARMA INGREDIENTS

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API Suppliers

API Suppliers

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USDMF

US DMFs Filed

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CEP/COS

CEP/COS Certifications

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JDMF

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EU WC

EU WC

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KDMF

KDMF

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NDC API

NDC API

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VMF

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Listed Suppliers

Other Suppliers

API REF. PRICE (USD/KG)

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$ 0

MARKET PLACE

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API

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FDF

0INTERMEDIATES

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FDA (Orange Book)

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Europe

Europe

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Australia

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South Africa

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Listed Dossiers

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DRUG PRODUCT COMPOSITIONS

REF. STANDARDS OR IMPURITIES

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USP

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JP

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PATENTS & EXCLUSIVITIES

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Data Compilation #PharmaFlow

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Stock Recap #PipelineProspector

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Weekly News Recap #Phispers

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News #PharmaBuzz

GLOBAL SALES INFORMATION

US Medicaid

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Annual Reports

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Finished Drug Prices

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0RELATED EXCIPIENT COMPANIES

0EXCIPIENTS BY APPLICATIONS

Chemistry

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FDF Dossiers

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01

Bayer AG

Germany
AES 2024
Not Confirmed
arrow

Bayer AG

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 250UNIT/VIAL

Packaging : 2.5ML

Approval Date :

Application Number : 2451441

Regulatory Info : Schedule D

Registration Country : Canada

blank

02

Bayer AG

Germany
AES 2024
Not Confirmed
arrow

Bayer AG

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 500UNIT/VIAL

Packaging : 2.5ML

Approval Date :

Application Number : 2451468

Regulatory Info : Schedule D

Registration Country : Canada

blank

03

Bayer AG

Germany
AES 2024
Not Confirmed
arrow

Bayer AG

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 1000UNIT/VIAL

Packaging : 2.5ML

Approval Date :

Application Number : 2451476

Regulatory Info : Schedule D

Registration Country : Canada

blank

04

Bayer AG

Germany
AES 2024
Not Confirmed
arrow

Bayer AG

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 2000UNIT/VIAL

Packaging : 5ML

Approval Date :

Application Number : 2451484

Regulatory Info : Schedule D

Registration Country : Canada

blank

05

Bayer AG

Germany
AES 2024
Not Confirmed
arrow

Bayer AG

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 3000UNIT/VIAL

Packaging : 5ML

Approval Date :

Application Number : 2451492

Regulatory Info : Schedule D

Registration Country : Canada

blank
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Canada

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01

BAYER INC

Germany
AES 2024
Not Confirmed
arrow

BAYER INC

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 250UNIT/VIAL

Packaging : 2.5ML

Approval Date :

Application Number : 2451441

Regulatory Info : Schedule D

Registration Country : Canada

blank

02

BAYER INC

Germany
AES 2024
Not Confirmed
arrow

BAYER INC

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 500UNIT/VIAL

Packaging : 2.5ML

Approval Date :

Application Number : 2451468

Regulatory Info : Schedule D

Registration Country : Canada

blank

03

BAYER INC

Germany
AES 2024
Not Confirmed
arrow

BAYER INC

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 1000UNIT/VIAL

Packaging : 2.5ML

Approval Date :

Application Number : 2451476

Regulatory Info : Schedule D

Registration Country : Canada

blank

04

BAYER INC

Germany
AES 2024
Not Confirmed
arrow

BAYER INC

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 2000UNIT/VIAL

Packaging : 5ML

Approval Date :

Application Number : 2451484

Regulatory Info : Schedule D

Registration Country : Canada

blank

05

BAYER INC

Germany
AES 2024
Not Confirmed
arrow

BAYER INC

Germany
arrow
AES 2024
Not Confirmed

ANTIHEMOPHILIC FACTOR (RECOMBINANT)

Brand Name : KOVALTRY

Dosage Form : KIT

Dosage Strength : 3000UNIT/VIAL

Packaging : 5ML

Approval Date :

Application Number : 2451492

Regulatory Info : Schedule D

Registration Country : Canada

blank
Full Screen ViewFULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

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