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01 8Aspen Pharma Trading Limited

02 22Care4 Aps

03 4ALFA WASSERMANN SpA

04 3BGP PRODUCTS Srl(GRUPPO MYLAN)

05 1Biane Ae

06 1Biomed Ag

07 3Gineladius S.L.

08 5Gineladius Sl

09 8ITALFARMACO SpA

10 20Leo Pharma A/S

11 1Mepha Pharma Ag

12 3Mylan Pharmaceuticals Limited

13 10Orifarm A/S

14 1Orifarm AS

15 10PFIZER AS

16 1PFIZER LTD (SANDWICH UK)

17 8Paranova Denmark A/S

18 12Pfizer AS

19 9Pfizer Ag

20 10Pfizer Aps

21 9Pfizer Sl

22 6Rovi Pharmaceutical Laboratories Sa

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine Forte

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 28-11-2000

Application Number : 63496

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 01-04-1998

Application Number : 61783

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine Forte

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 28-11-2000

Application Number : 63498

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 01-06-1991

Application Number : 58983

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 01-11-1989

Application Number : 58496

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine Forte

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 28-11-2000

Application Number : 63497

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine

Dosage Form : Injectable Solution

Dosage Strength :

Packaging :

Approval Date : 01-06-1991

Application Number : 58982

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAspen API. More than just an API™

Regulatory Info : Cancelled

Registration Country : Spain

Nadroparin Calcium

Brand Name : Fraxiparine

Dosage Form : Injectable Solution

Dosage Strength : 9500IU

Packaging :

Approval Date : 02-06-2021

Application Number : 86000

Regulatory Info : Cancelled

Registration Country : Spain

Aspen API Comapny Banner

09

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Tinzaparin Sodium

Brand Name : Innohep

Dosage Form : Solution For Injection

Dosage Strength : 10.000 anti-Xa IU

Packaging :

Approval Date : 25-01-2013

Application Number : 28105840512

Regulatory Info : Prescription

Registration Country : Denmark

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10

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Tinzaparin Sodium

Brand Name : Innohep

Dosage Form : Solution For Injection

Dosage Strength : 14.000 anti-Xa IU

Packaging :

Approval Date : 25-01-2013

Application Number : 28105840612

Regulatory Info : Prescription

Registration Country : Denmark

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