Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 2,506Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 3Mankind Pharma

02 1Abacus Medicine

03 3Alembic Pharmaceuticals Limited

04 5Apotex Inc

05 4Aspire Pharma Limited

06 3Aurobindo Pharma Limited

07 1BONISCONTRO & GAZZONE Srl

08 11Brancaster Pharma Ireland Ltd.

09 3Chartwell Pharmaceuticals llc

10 3Cheplapharm Arzneimittel Gmbh

11 1Ebb Medical

12 2Evolan Pharma AB

13 3IST.LUSOFARMACO D'ITALIA SpA

14 3Impax Laboratories

15 2JAMP PHARMA

16 2Leman Skl Sa

17 2MANTRA PHARMA INC

18 2MARCAN PHARMACEUTICALS INC

19 1Medartuum

20 4Medical Valley

21 1Myungmoon Pharm. Co., LTD.

22 3Novugen

23 2ORIFARM GROUP AS

24 3PH HEALTH

25 3Rubicon Research

26 2SANIS HEALTH INC

27 3Shijiazhuang Yiling Pharmaceutical Co.,Ltd.

28 1Smith & Kenner Pharmaceuticals

29 2Substipharm

30 3THINQ Pharma-CRO PVT Ltd

31 3Takeda Pharmaceutical

32 4Tillomed Laboratories Ltd

33 1UNION HEALTH Srl

34 3Viatris

35 3Xiromed

36 4Zentiva

37 3Zydus Lifesciences

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : RX

Registration Country : USA

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2023-11-01

Application Number : 217271

Regulatory Info : RX

Registration Country : USA

Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : RX

Registration Country : USA

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2023-11-01

Application Number : 217271

Regulatory Info : RX

Registration Country : USA

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : RX

Registration Country : USA

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2023-11-01

Application Number : 217271

Regulatory Info : RX

Registration Country : USA

Company Banner

04

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2006-09-12

Application Number : 77746

Regulatory Info : RX

Registration Country : USA

blank

05

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2006-09-12

Application Number : 77746

Regulatory Info : RX

Registration Country : USA

blank

06

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2003-09-11

Application Number : 76514

Regulatory Info : DISCN

Registration Country : USA

blank

07

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2003-09-11

Application Number : 76514

Regulatory Info : DISCN

Registration Country : USA

blank

08

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2004-07-02

Application Number : 76514

Regulatory Info : DISCN

Registration Country : USA

blank

09

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2004-05-27

Application Number : 76449

Regulatory Info : RX

Registration Country : USA

blank

10

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2004-05-27

Application Number : 76449

Regulatory Info : RX

Registration Country : USA

blank

11

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2005-12-16

Application Number : 76449

Regulatory Info : RX

Registration Country : USA

blank

12

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : ORVATEN

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2004-11-03

Application Number : 76725

Regulatory Info : RX

Registration Country : USA

blank

13

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : ORVATEN

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2004-11-03

Application Number : 76725

Regulatory Info : RX

Registration Country : USA

blank

14

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : ORVATEN

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2004-11-03

Application Number : 76725

Regulatory Info : RX

Registration Country : USA

blank

15

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : PROAMATINE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-09-06

Application Number : 19815

Regulatory Info : DISCN

Registration Country : USA

blank

16

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : PROAMATINE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-09-06

Application Number : 19815

Regulatory Info : DISCN

Registration Country : USA

blank

17

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : PROAMATINE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2002-03-20

Application Number : 19815

Regulatory Info : DISCN

Registration Country : USA

blank

18

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2003-09-10

Application Number : 76577

Regulatory Info : RX

Registration Country : USA

blank

19

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2003-09-10

Application Number : 76577

Regulatory Info : RX

Registration Country : USA

blank

20

Asia Pharma Expo
Not Confirmed
arrow
arrow
Asia Pharma Expo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2003-09-10

Application Number : 76577

Regulatory Info : RX

Registration Country : USA

blank