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Lasmiditan Hemisuccinate
FDF Dossiers

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Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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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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As a CDMO, Mikart offers integrated CDMO services for Solid Dose & Non-sterile Liquid formulations.

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Lasmiditan hemisuccinate

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

12 API Suppliers, 4 USDMF, 1 KDMF, 2 NDC API, 9 Listed Suppliers, $ API Reference Price

12 API Suppliers
4 USDMF
1 KDMF
2 NDC API
9 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

8 Drugs in Development

8 Drugs in Development

INTERMEDIATES

2 Intermediate Suppliers

2 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

5 FDF Dossiers, 5 FDA Orange Book

5 FDF Dossiers
5 FDA Orange Book

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow, 16 NEWS #PharmaBuzz

1 DATA COMPILATION #PharmaFlow
16 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

1 US Medicaid Prescriptions

1 US Medicaid Prescriptions

MARKET PLACE

6 APIs

6 APIs

PATENTS & EXCLUSIVITIES

8 US Patents, 3 US Exclusivities

8 US Patents
3 US Exclusivities

$ API Ref.Price (USD/KG) : 2,989 Xls

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5 All

01 3Eli Lilly

02 2QILU PHARMACEUTICAL CO., LTD.

filter Dosage Reset all filters

5 All

01 2TABLET

02 3TABLET;ORAL

filter Regulatory Info Reset all filters

5 All

01 1DISCN

02 2RX

03 2Blank

filter Brand Name Reset all filters

5 All

01 2LASMIDITAN

02 3REYVOW

filter Country Reset all filters

5 All

01 5USA

Metrochem LASMIDITAN

List of Suppliers

Product Main Page

01

Eli Lilly

AAM

Not Confirmed

Eli Lilly

AAM

Not Confirmed

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Digital Content

Regulatory Info : RX

Registration Country : USA

LASMIDITAN SUCCINATE

Brand Name : REYVOW

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 2020-01-31

Application Number : 211280

Regulatory Info : RX

Registration Country : USA

Portfolio PDF

Product Web Link

Digital Content

02

Eli Lilly

AAM

Not Confirmed

Eli Lilly

AAM

Not Confirmed

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Digital Content

Regulatory Info : RX

Registration Country : USA

LASMIDITAN SUCCINATE

Brand Name : REYVOW

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2020-01-31

Application Number : 211280

Regulatory Info : RX

Registration Country : USA

Portfolio PDF

Product Web Link

Digital Content

03

Eli Lilly

AAM

Not Confirmed

Eli Lilly

AAM

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

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Digital Content

Regulatory Info : DISCN

Registration Country : USA

LASMIDITAN SUCCINATE

Brand Name : REYVOW

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2020-12-18

Application Number : 211280

Regulatory Info : DISCN

Registration Country : USA

Portfolio PDF

Product Web Link

Digital Content

04

QILU PHARMACEUTICAL CO., LTD.

Country

AAM

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QILU PHARMACEUTICAL CO., LTD.

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AAM

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Regulatory Info :

Registration Country : USA

Brand Name : LASMIDITAN

Dosage Form : TABLET

Dosage Strength : 100MG

Packaging :

Approval Date :

Application Number : 219350

Regulatory Info :

Registration Country : USA

Portfolio PDF

Product Web Link

Virtual Booth

Digital Content

Website

Corporate PDF

05

QILU PHARMACEUTICAL CO., LTD.

Country

AAM

Not Confirmed

QILU PHARMACEUTICAL CO., LTD.

Country

AAM

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

Post an Enquiry

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Country

Virtual Booth

Digital Content

Regulatory Info :

Registration Country : USA

Brand Name : LASMIDITAN

Dosage Form : TABLET

Dosage Strength : 50MG

Packaging :

Approval Date :

Application Number : 219350

Regulatory Info :

Registration Country : USA

Portfolio PDF

Product Web Link

Virtual Booth

Digital Content

Website

Corporate PDF

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