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01 3Mankind Pharma

02 3Alembic Pharmaceuticals Limited

03 5Apotex Inc

04 2Aspire Pharma Limited

05 3Aurobindo Pharma Limited

06 1BONISCONTRO & GAZZONE Srl

07 8Brancaster Pharma Ireland Ltd.

08 3Chartwell Pharmaceuticals llc

09 3Cheplapharm Arzneimittel Gmbh

10 3IST.LUSOFARMACO D'ITALIA SpA

11 3Impax Laboratories

12 2JAMP PHARMA

13 2Leman Skl Sa

14 2MANTRA PHARMA INC

15 2MARCAN PHARMACEUTICALS INC

16 2Medical Valley

17 1Myungmoon Pharm. Co., LTD.

18 3Novugen

19 2ORIFARM GROUP AS

20 3PH HEALTH

21 3Rubicon Research

22 2SANIS HEALTH INC

23 3Shijiazhuang Yiling Pharmaceutical Co.,Ltd.

24 1Smith & Kenner Pharmaceuticals

25 2Substipharm

26 3THINQ Pharma-CRO PVT Ltd

27 3Takeda Pharmaceutical

28 2Tillomed Laboratories Ltd

29 1UNION HEALTH Srl

30 3Viatris

31 3Xiromed

32 2Zentiva

33 3Zydus Lifesciences

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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

ASPEN
Not Confirmed
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ASPEN
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

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05

ASPEN
Not Confirmed
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ASPEN
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

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06

ASPEN
Not Confirmed
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ASPEN
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

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07

ASPEN
Not Confirmed
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ASPEN
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

ASPEN
Not Confirmed
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ASPEN
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

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09

ASPEN
Not Confirmed
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ASPEN
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

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10

ASPEN
Not Confirmed
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ASPEN
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

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11

ASPEN
Not Confirmed
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ASPEN
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

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12

ASPEN
Not Confirmed
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ASPEN
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

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13

ASPEN
Not Confirmed
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ASPEN
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

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14

ASPEN
Not Confirmed
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ASPEN
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

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15

ASPEN
Not Confirmed
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ASPEN
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

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16

ASPEN
Not Confirmed
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ASPEN
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

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17

ASPEN
Not Confirmed
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ASPEN
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

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18

ASPEN
Not Confirmed
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ASPEN
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

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19

ASPEN
Not Confirmed
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ASPEN
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

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20

ASPEN
Not Confirmed
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ASPEN
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

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