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01 3Omgene Life Sciences Pvt. Ltd

02 4Naprod Life Sciences

03 2Ascent Innovative Medicines

04 5Avet Pharmaceuticals

05 5Bioindustria L.I.M. Spa

06 3Biological E

07 1CHIESI USA INC

08 4Campus Pharma AB

09 6Chemi SpA

10 1Farmak JSC

11 2Flagship Biotech International Pvt. Ltd

12 6Fresenius Kabi AB Brunna

13 5Fresenius Kabi USA

14 4GLAND PHARMA LIMITED

15 3GP Pharm

16 12Generic Health

17 1Hainan Shuangcheng Pharmaceuticals

18 12Hospira, Inc.

19 7Italfarmaco S.p.A

20 3LIFEPHARMA SpA

21 4Labatec Pharm

22 3Lifepharma

23 5Meitheal Pharmaceuticals

24 3Mepha Pharma

25 2Montage Laboratories

26 1NordicInfu Care AB

27 3Northern Medical Group ApS

28 42Novartis Pharmaceuticals Corporation

29 2ORIFARM GROUP AS

30 4Omega Laboratories Limited

31 3Pluviaendo

32 5Sagent Pharmaceuticals

33 33Sun Pharmaceutical Industries Limited

34 12Teva Pharma Australia

35 8Teva Pharmaceutical Industries

36 1Varian Pharmed

37 3Viatris

38 5West-ward Pharmaceutical Corp

39 5Wockhardt

40 7Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOmgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Injectable Suspension

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Omgene Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 50MCG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOmgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Injectable Suspension

Dosage Strength : 20MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Omgene Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOmgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Injectable Suspension

Dosage Strength : 30MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Omgene Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 100MCG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 200MCG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Octreotide Acetate

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 500MCG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

08

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : OCTREOTIDE ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.05MG BASE/ML

Packaging :

Approval Date : 2005-10-03

Application Number : 75957

Regulatory Info : RX

Registration Country : USA

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09

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : OCTREOTIDE ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML

Packaging :

Approval Date : 2005-10-03

Application Number : 75957

Regulatory Info : RX

Registration Country : USA

blank

10

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : OCTREOTIDE ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.5MG BASE/ML

Packaging :

Approval Date : 2005-10-03

Application Number : 75957

Regulatory Info : RX

Registration Country : USA

blank

11

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : OCTREOTIDE ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.2MG BASE/ML

Packaging :

Approval Date : 2005-11-21

Application Number : 75959

Regulatory Info : RX

Registration Country : USA

blank

12

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : OCTREOTIDE ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML

Packaging :

Approval Date : 2005-11-21

Application Number : 75959

Regulatory Info : RX

Registration Country : USA

blank

13

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.05MG BASE/ML

Packaging :

Approval Date : 1988-10-21

Application Number : 19667

Regulatory Info : RX

Registration Country : USA

blank

14

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.1MG BASE/ML

Packaging :

Approval Date : 1988-10-21

Application Number : 19667

Regulatory Info : RX

Registration Country : USA

blank

15

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.5MG BASE/ML

Packaging :

Approval Date : 1988-10-21

Application Number : 19667

Regulatory Info : RX

Registration Country : USA

blank

16

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-06-12

Application Number : 19667

Regulatory Info : DISCN

Registration Country : USA

blank

17

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-06-12

Application Number : 19667

Regulatory Info : DISCN

Registration Country : USA

blank

18

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN LAR

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/VIAL

Packaging :

Approval Date : 1998-11-25

Application Number : 21008

Regulatory Info : RX

Registration Country : USA

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19

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN LAR

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG BASE/VIAL

Packaging :

Approval Date : 1998-11-25

Application Number : 21008

Regulatory Info : RX

Registration Country : USA

blank

20

FCE Pharma
Not Confirmed
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FCE Pharma
Not Confirmed

OCTREOTIDE ACETATE

Brand Name : SANDOSTATIN LAR

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 30MG BASE/VIAL

Packaging :

Approval Date : 1998-11-25

Application Number : 21008

Regulatory Info : RX

Registration Country : USA

blank