Aspen API. More than just an API™
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01 8Aspen API
02 6Aspen Pharmacare Holdings
03 82care4
04 1Abacus Medicine
05 5Abbott Laboratories
06 5Acino Pharma (Pty) Ltd
07 4Alfasigma
08 3BGP Group of Companies
09 1Biane Ae
10 5Biological E
11 1Biomed
12 2Flagship Biotech International Pvt. Ltd
13 5Gineladius Sl
14 8Italfarmaco S.p.A
15 6Laboratorios Farmaceuticos Rovi
16 34Leo Pharma
17 4Medartuum
18 1Mepha Pharma
19 1Northern Medical Group Aps
20 12ORIFARM GROUP AS
21 1Oasmia Pharmaceutical
22 6Paranova Pharmaceuticals Ab
23 55Pfizer Inc
24 2Pharmachim Ab
25 2Unimedic AB
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01 11.750Reviparina Iu 0.25Ml 10 Units Parenteral Use
02 14.250Parnaparin Iu Axa 0.4 Ml 6 Units Parenteral Use
03 16.300Reviparina Iu 0,9Ml 10 Units Parenteral Use
04 16.400Parnaparin Iu Axa 0,6Ml 6 Units Parenteral Use
05 18.500Parnaparin Iu Axa 0,8Ml 6 Units Parenteral Use
06 1Cream
07 1Dalteparin 100.000Iu 1 Unit Parenteral Use
08 1Gel
09 6INJ
10 4INJECTABLE;INJECTION
11 11INJECTABLE;SUBCUTANEOUS
12 38Injectable Solution
13 1Injectable Solution In Ampoule
14 7Injectable Solution In Pre-Filled Syringe
15 1Injectable Solution In Vial
16 2Injection
17 1Nadroparin 11.400Iu 2 Units Parenteral Use
18 1Nadroparin 15.200Iu 2 Units Parenteral Use
19 1Nadroparin 19.000Iu 2 Units Parenteral Use
20 1Nadroparin 2.850Iu Axa/0,3Ml 6 Units Parenteral Use
21 1Nadroparin 3.800Iu 6 Units Parenteral Use
22 1Nadroparin 5.700Iu 10 Units Parenteral Use
23 1Nadroparin 7.600Iu 10 Units Parenteral Use
24 1Nadroparin 9.500Iu 10 Units Parenteral Use
25 1Parnaparin 3,200 Iu Axa 0,3Ml 6 Units Parenteral Use
26 3Pre Filled Syringe
27 1Reviparina 4,200 Iu 0,6Ml 10 Units Parenteral Use
28 5SOL
29 21SOLUTION
30 3Solution
31 64Solution For Injection
32 2Vial
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01 11Allowed
02 22Approved
03 27Authorized
04 10Cancelled
05 6DISCN
06 45Deregistered
07 2Generic
08 11Originator
09 21Prescription
10 9RX
11 1Suspensed
12 21Blank
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01 3Clivarina
02 5Clivarine
03 1Dalteparin Sodium Pfizer
04 1Dolobene
05 1Entervit
06 22FRAGMIN
07 4Fluxum
08 10Fragmin
09 5Fragmin
10 4Fragmin IE
11 4Fragmin (With Preservative)
12 43Fragmine
13 5Fraxiparine
14 1Fraxiparine 0.2ml
15 1Fraxiparine 0.3ml
16 1Fraxiparine 0.4ml
17 1Fraxiparine 0.6ml
18 1Fraxiparine 0.8ml
19 1Fraxiparine 1.0ml
20 3Fraxiparine Forte
21 1Hepadren
22 7Hibor
23 1Hibor 10000 I.U./0,4 ml
24 1Hibor 2500 I.U./0,2 ml
25 1Hibor 3500 I.U./0,2 ml
26 1Hibor 5000 I.U./0,2 ml
27 1Hibor 7500 I.U./0,3 ml
28 12INNOHEP
29 23Innohep
30 2NORMIFLO
31 3Phivor
32 3Seledie
33 5Seleparina
34 1Sensicutan
35 7Blank
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01 21Canada
02 7India
03 16Italy
04 11South Africa
05 38Spain
06 67Sweden
07 11Switzerland
08 15USA
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine Forte
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 2000-11-28
Application Number : 63496
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.8ml
Dosage Form : INJ
Dosage Strength : 7600iu/0.8ml
Packaging : 0.8X10iu/0.8ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1998-04-01
Application Number : 61783
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine Forte
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 2000-11-28
Application Number : 63498
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1991-06-01
Application Number : 58983
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1989-11-01
Application Number : 58496
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine Forte
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 2000-11-28
Application Number : 63497
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength :
Packaging :
Approval Date : 1991-06-01
Application Number : 58982
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Fraxiparine
Dosage Form : Injectable Solution
Dosage Strength : 9500IU
Packaging :
Approval Date : 2021-06-02
Application Number : 86000
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 1.0ml
Dosage Form : INJ
Dosage Strength : 9500iu/1ml
Packaging : 1X10iu/1ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.2ml
Dosage Form : INJ
Dosage Strength : 1900iu/0.2ml
Packaging : 0.2X10iu/0.2ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.3ml
Dosage Form : INJ
Dosage Strength : 2850iu/0.3ml
Packaging : 0.3X10iu/0.3ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.4ml
Dosage Form : INJ
Dosage Strength : 3800iu/0.4ml
Packaging : 0.4X10iu/0.4ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fraxiparine 0.6ml
Dosage Form : INJ
Dosage Strength : 5700iu/0.6ml
Packaging : 0.6X10iu/0.6ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORMIFLO
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10,000 UNITS/0.5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-05-23
Application Number : 20227
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORMIFLO
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 5,000 UNITS/0.5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-05-23
Application Number : 20227
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FRAGMIN
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 2,500IU/0.2ML (12,500IU/ML)
Packaging :
Approval Date : 1994-12-22
Application Number : 20287
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FRAGMIN
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 10,000IU/0.4ML (25,000IU/ML)
Packaging :
Approval Date : 2007-05-01
Application Number : 20287
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FRAGMIN
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 5,000IU/0.2ML (25,000IU/ML)
Packaging :
Approval Date : 1996-03-18
Application Number : 20287
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FRAGMIN
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 10,000IU/ML (10,000IU/ML)
Packaging :
Approval Date : 1998-01-30
Application Number : 20287
Regulatory Info : RX
Registration Country : USA