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01 3Alembic Pharmaceuticals Limited

02 5Apotex Inc

03 3Aurobindo Pharma Limited

04 1BONISCONTRO & GAZZONE Srl

05 4CPS Cito Pharma Services GmbH

06 3Chartwell Pharmaceuticals llc

07 3ENDO OPERATIONS

08 3IST.LUSOFARMACO D'ITALIA SpA

09 3Impax Laboratories

10 2JAMP PHARMA

11 2MARCAN PHARMACEUTICALS INC

12 3Mankind Pharma

13 1Myungmoon Pharm. Co., LTD.

14 3Novugen

15 3Rubicon Research

16 2SANIS HEALTH INC

17 1Smith & Kenner Pharmaceuticals

18 2Substipharm

19 3THINQ Pharma-CRO PVT Ltd

20 3Takeda Pharmaceutical

21 1UNION HEALTH Srl

22 3Upsher-Smith Laboratories

23 3Viatris

24 3Xiromed

25 3Zydus Lifesciences

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PharmaCompass

01

PackExpo
Not Confirmed
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PackExpo
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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02

PackExpo
Not Confirmed
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PackExpo
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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03

PackExpo
Not Confirmed
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PackExpo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2006-09-12

Application Number : 77746

Regulatory Info : RX

Registration Country : USA

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04

PackExpo
Not Confirmed
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PackExpo
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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05

PackExpo
Not Confirmed
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PackExpo
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

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06

PackExpo
Not Confirmed
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PackExpo
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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07

PackExpo
Not Confirmed
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PackExpo
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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08

PackExpo
Not Confirmed
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PackExpo
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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09

PackExpo
Not Confirmed
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PackExpo
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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10

PackExpo
Not Confirmed
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PackExpo
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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11

PackExpo
Not Confirmed
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PackExpo
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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12

PackExpo
Not Confirmed
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PackExpo
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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13

PackExpo
Not Confirmed
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PackExpo
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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14

PackExpo
Not Confirmed
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PackExpo
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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15

PackExpo
Not Confirmed
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PackExpo
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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16

PackExpo
Not Confirmed
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PackExpo
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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17

PackExpo
Not Confirmed
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PackExpo
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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18

PackExpo
Not Confirmed
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PackExpo
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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19

ENDO OPERATIONS

Country
PackExpo
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ENDO OPERATIONS

Country
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MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG

Packaging :

Approval Date : 2018-10-29

Application Number : 207169

Regulatory Info : RX

Registration Country : USA

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20

ENDO OPERATIONS

Country
PackExpo
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ENDO OPERATIONS

Country
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PackExpo
Not Confirmed

MIDODRINE HYDROCHLORIDE

Brand Name : MIDODRINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2018-10-29

Application Number : 207169

Regulatory Info : RX

Registration Country : USA

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