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01 3Dr. Reddy's Laboratories

02 1Biophore India Pharmaceuticals Pvt Ltd

03 1Orion Corporation

04 3Pharmathen SA

05 1Altan Pharma

06 5American Regent

07 3Amphastar Pharmaceuticals

08 1Bahrain Pharma

09 2Bharat Parenterals Limited

10 1Biem Ilac San. ve Tic. A.S

11 1Bio Labs

12 2Brooks laboratories Limited

13 1COOPER PHARMA

14 9CSL Vifor

15 1Clinigen Group

16 1Cogmill Pharma Ab

17 1Flagship Biotech International Pvt. Ltd

18 1Fresenius Medical Care de Mexico

19 1GEYMONAT SpA

20 2Health Biotech

21 1INNOVATA PHARMACEUTICALS

22 1Ind Swift Laboratories Limited

23 1Lifespan Biotech

24 1Luitpold Pharmaceuticals, Inc.

25 1MS Pharma

26 1Madras Pharmaceuticals

27 1Maiva Pharma

28 2Medartuum

29 1Montage Laboratories

30 9ORIFARM GROUP AS

31 2Omnia L?kemedel Ab

32 1Opes Health Care

33 3Paranova Pharmaceuticals Ab

34 2Pharmachim Ab

35 1Pharmada Pharmaceuticals

36 1Pharmascience Inc.

37 1Rechon Life Science

38 4Sandoz B2B

39 6Seqirus

40 1Stanex Drugs and Chemicals

41 1Themis Medicare

42 2Unimedic AB

43 1Vefa Ilac

44 3Viatris

45 1World Medicine

46 1Zydus Healthcare

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Iron Sucrose

Brand Name :

Dosage Form : Injection

Dosage Strength : 100MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

SUCROFERRIC OXYHYDROXIDE

Brand Name :

Dosage Form : Tablet

Dosage Strength : 500MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Biophore

03

Iron Sucrose

Brand Name : Holiday

Dosage Form : Solution For Injection

Dosage Strength : 20mg/ml

Packaging :

Approval Date : 11/12/2009

Application Number : 20080307000013

Regulatory Info : Deregistered

Registration Country : Sweden

Fermion Orion Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : USA

Registration Country : Greece

Sucroferric Oxyhydroxide

Brand Name :

Dosage Form : Injection For Intravenous Use

Dosage Strength : 50MG/2.5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : USA

Registration Country : Greece

Pharmathen

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Iron Sucrose

Brand Name :

Dosage Form : Injection

Dosage Strength : 200MG/10ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Iron Sucrose

Brand Name :

Dosage Form : Injection

Dosage Strength : 50MG/2.5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : USA

Registration Country : Greece

Sucroferric Oxyhydroxide

Brand Name :

Dosage Form : Injection For Intravenous Use

Dosage Strength : 100MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : USA

Registration Country : Greece

Pharmathen

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

Regulatory Info : USA

Registration Country : Greece

Sucroferric Oxyhydroxide

Brand Name :

Dosage Form : Injection For Intravenous Use

Dosage Strength : 200MG/10ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : USA

Registration Country : Greece

Pharmathen

09

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : VENOFER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 100MG IRON/5ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2000-11-06

Application Number : 21135

Regulatory Info : RX

Registration Country : USA

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10

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : VENOFER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 50MG IRON/2.5ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2005-03-20

Application Number : 21135

Regulatory Info : RX

Registration Country : USA

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11

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : VENOFER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 75MG IRON/3.75ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2005-03-29

Application Number : 21135

Regulatory Info : DISCN

Registration Country : USA

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12

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : VENOFER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 200MG IRON/10ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2007-02-09

Application Number : 21135

Regulatory Info : RX

Registration Country : USA

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13

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : VENOFER

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 65MG IRON/3.25ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2013-03-29

Application Number : 21135

Regulatory Info : DISCN

Registration Country : USA

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14

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : IRON SUCROSE

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 50MG IRON/2.5ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2025-08-08

Application Number : 208977

Regulatory Info : RX

Registration Country : USA

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15

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : IRON SUCROSE

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 100MG IRON/5ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2025-08-08

Application Number : 208977

Regulatory Info : RX

Registration Country : USA

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16

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : IRON SUCROSE

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 200MG IRON/10ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2025-08-08

Application Number : 208977

Regulatory Info : RX

Registration Country : USA

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17

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

FERRIC OXYHYDROXIDE

Brand Name : VELPHORO

Dosage Form : TABLET, CHEWABLE;ORAL

Dosage Strength : EQ 500MG IRON

Packaging :

Approval Date : 2013-11-27

Application Number : 205109

Regulatory Info : RX

Registration Country : USA

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18

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : IRON SUCROSE

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 50MG IRON/2.5ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2025-08-08

Application Number : 212340

Regulatory Info : RX

Registration Country : USA

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19

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : IRON SUCROSE

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 100MG IRON/5ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2025-08-08

Application Number : 212340

Regulatory Info : RX

Registration Country : USA

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20

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

IRON SUCROSE

Brand Name : IRON SUCROSE

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 200MG IRON/10ML (EQ 20MG IRON/ML)

Packaging :

Approval Date : 2025-08-08

Application Number : 212340

Regulatory Info : RX

Registration Country : USA

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