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01 3Orion Corporation

02 1Dr. Reddy's Laboratories

03 1Octavius Pharma Pvt. Ltd

04 3Sumar Biotech

05 82care4

06 1AAIPharma Services Corp.

07 2ABHAI LLC

08 2Acerus Pharmaceuticals

09 4Actavis Inc

10 3Adalvo

11 1American Regent

12 5Apotex Inc

13 6Aristo Pharma GmbH

14 2Ascent Innovative Medicines

15 2Aspire Pharma Limited

16 2Aurobindo Pharma Limited

17 2Avet Pharmaceuticals

18 2BEDFORD LABS

19 1Bausch & Lomb Incorporated

20 2Cantabria Labs

21 3Central Procurement & Supplies Unit

22 1Cherubino Limited

23 1Ebb Medical

24 4Farbe Firma

25 3Farmacia Nordic Ab

26 2Farmak JSC

27 2Farmatek

28 5Ferring Ireland Limited

29 128Ferring Pharmaceuticals

30 2GLAND PHARMA LIMITED

31 2GP Pharm

32 6Gebro Pharma

33 2Glenmark Pharmaceuticals

34 1Health House Pharma Ltd T/As P&D Pharmaceuticals Ltd

35 1Hospira, Inc.

36 2Impax Laboratories

37 2Jeil Pharmaceutical Co., Ltd

38 1KVR Pharmaceuticals

39 3Karo Pharma

40 2Kedrion

41 2Medartuum

42 2Medsurge Healthcare

43 1Meitheal Pharmaceuticals

44 2NTC

45 2Natco Pharma

46 12Newbury Pharmaceuticals AB

47 3Newbury Pharmaceuticals Ab

48 2Nordic Pharma

49 1Nordic Pill Ab

50 2Novast Laboratories

51 11ORIFARM GROUP AS

52 1P & D Pharmaceuticals Limited

53 3PHAGECON

54 3Parallel Pharma Ab

55 2Paranova Pharmaceuticals Ab

56 4Pharmascience Inc.

57 1Raha Pharmaceutical Co

58 2Reig Jofre

59 10STADA Arzneimittel

60 2Sagent Pharmaceuticals

61 10Sandoz B2B

62 3Sun Pharmaceutical Industries Limited

63 1Supremeuni

64 7Teva Pharmaceutical Industries

65 2UBI Pharma

66 1Unimedic AB

67 1West-Coast Pharmaceuticals

68 9Zentiva

69 1Zydus Pharmaceuticals

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PharmaCompass

01

Desmopressin Acetate

Brand Name : Desmopressin Orion

Dosage Form : Sublingual Tablet

Dosage Strength : 120mcg

Packaging :

Approval Date : 06/10/2023

Application Number : 20220628000051

Regulatory Info : Approved

Registration Country : Sweden

Fermion Orion Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : RX

Registration Country : USA

DESMOPRESSIN ACETATE

Brand Name : DESMOPRESSIN ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.004MG/ML

Packaging :

Approval Date : 2022-08-19

Application Number : 215961

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOctavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.

Regulatory Info :

Registration Country : India

Desmopressin Acetate

Brand Name : Desmopressin Acetate

Dosage Form : Intranasal Solution

Dosage Strength : 0.01%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSumar Biotech work together to Innovate & Manufacture Semi-synthetic, Synthetic & Fermentation API.

Regulatory Info : Authorised

Registration Country : Malta

Desmopressin

Brand Name : Desmopressin Sumar

Dosage Form : Sublingual Tablet

Dosage Strength : 60MCG

Packaging :

Approval Date : 2023-01-16

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

Sumar Biotech

05

Desmopressin Acetate

Brand Name : Desmopressin Orion

Dosage Form : Sublingual Tablet

Dosage Strength : 240mcg

Packaging :

Approval Date : 06/10/2023

Application Number : 20220628000068

Regulatory Info : Approved

Registration Country : Sweden

Fermion Orion Company Banner

06

Desmopressin Acetate

Brand Name : Desmopressin Orion

Dosage Form : Sublingual Tablet

Dosage Strength : 60mcg

Packaging :

Approval Date : 06/10/2023

Application Number : 20220628000044

Regulatory Info : Approved

Registration Country : Sweden

Fermion Orion Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSumar Biotech work together to Innovate & Manufacture Semi-synthetic, Synthetic & Fermentation API.

Regulatory Info : Authorised

Registration Country : Malta

Desmopressin

Brand Name : Desmopressin Sumar

Dosage Form : Sublingual Tablet

Dosage Strength : 120MCG

Packaging :

Approval Date : 2023-01-16

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

Sumar Biotech

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSumar Biotech work together to Innovate & Manufacture Semi-synthetic, Synthetic & Fermentation API.

Regulatory Info : Authorised

Registration Country : Malta

Desmopressin

Brand Name : Desmopressin Sumar

Dosage Form : Sublingual Tablet

Dosage Strength : 240MCG

Packaging :

Approval Date : 2023-01-16

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

Sumar Biotech

09

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

Desmopressin Acetate

Brand Name : Minirin

Dosage Form : Nasal Drop

Dosage Strength : 0.1mg/ml

Packaging :

Approval Date : 20/11/2019

Application Number : 20190705000109

Regulatory Info : Deregistered

Registration Country : Sweden

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10

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

Desmopressin Acetate

Brand Name : Desmopresina Aristo

Dosage Form : Sublingual Tablet

Dosage Strength : 60MCG

Packaging :

Approval Date : 2023-08-23

Application Number : 89024

Regulatory Info : Authorized

Registration Country : Spain

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11

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

Desmopressin Acetate

Brand Name : Desmopresina Aristo

Dosage Form : Sublingual Tablet

Dosage Strength : 240MCG

Packaging :

Approval Date : 2023-08-23

Application Number : 89023

Regulatory Info : Authorized

Registration Country : Spain

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12

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

DESMOPRESSIN ACETATE

Brand Name : DDAVP

Dosage Form : SOLUTION;NASAL

Dosage Strength : 0.01%

Packaging :

Approval Date : 1982-01-01

Application Number : 17922

Regulatory Info : DISCN

Registration Country : USA

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13

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

DESMOPRESSIN ACETATE

Brand Name : DDAVP

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1989-02-06

Application Number : 17922

Regulatory Info : DISCN

Registration Country : USA

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14

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

DESMOPRESSIN ACETATE

Brand Name : DDAVP (NEEDS NO REFRIGERATION)

Dosage Form : SPRAY, METERED;NASAL

Dosage Strength : 0.01MG/SPRAY

Packaging :

Approval Date : 1996-08-07

Application Number : 17922

Regulatory Info : DISCN

Registration Country : USA

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15

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

DESMOPRESSIN ACETATE

Brand Name : CONCENTRAID

Dosage Form : SOLUTION;NASAL

Dosage Strength : 0.01%

Packaging :

Approval Date : 1990-12-26

Application Number : 19776

Regulatory Info : DISCN

Registration Country : USA

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16

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

Desmopressin Acetate

Brand Name : Minirin

Dosage Form : Nasal Drop

Dosage Strength : 0.1mg/ml

Packaging :

Approval Date : 10/05/1974

Application Number : 19740510000029

Regulatory Info : Deregistered

Registration Country : Sweden

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17

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

Desmopressin Acetate

Brand Name : Minurin

Dosage Form : Injectable Solution

Dosage Strength : 4MCG

Packaging :

Approval Date : 1997-09-01

Application Number : 61413

Regulatory Info : Authorized

Registration Country : Spain

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18

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

Desmopressin Acetate

Brand Name : Minurin Flas

Dosage Form : Oral Lyophilized

Dosage Strength : 120MCG

Packaging :

Approval Date : 2006-12-15

Application Number : 68268

Regulatory Info : Authorized

Registration Country : Spain

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19

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

DESMOPRESSIN ACETATE

Brand Name : DDAVP

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.004MG/ML

Packaging :

Approval Date : 1984-03-30

Application Number : 18938

Regulatory Info : RX

Registration Country : USA

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20

COMPAMED
Not Confirmed
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COMPAMED
Not Confirmed

DESMOPRESSIN ACETATE

Brand Name : DDAVP

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.015MG/ML

Packaging :

Approval Date : 1995-04-25

Application Number : 18938

Regulatory Info : DISCN

Registration Country : USA

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