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

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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
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01 1Oral Drops
02 11TABLET
03 45TABLET;ORAL
04 41Tablet
05 5Blank
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01 4Allowed
02 16Approved
03 1Authorized
04 6DISCN
05 1Generic Reference drug
06 3Marketed
07 2Not Marketed
08 23Prescription
09 39RX
10 8Blank
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01 2APO-MIDODRINE
02 2Augermid
03 2Augermite
04 6Gutron
05 13Hypotron
06 2JAMP MIDODRINE
07 2M-MIDODRINE
08 2MAR-MIDODRINE
09 2MIDODRINE
10 39MIDODRINE HYDROCHLORIDE
11 1Midodrin Abacus Medicine
12 1Midodrin Leman
13 2Midodrin "Zentiva"
14 1Midodrina A.
15 1Midodrine Ebb
16 2Midodrine Evolan
17 1Midodrine Leman
18 1Midodrine Medartuum
19 2Midodrine Medical Valley
20 2Midodrine Tillomed
21 2Midodrine Zentiva
22 2Midodrine "Medical Valley"
23 2Midodrine "Tillomed"
24 1Midron
25 3ORVATEN
26 3PROAMATINE
27 1Xerotil
28 3Blank
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01 10Canada
02 13Denmark
03 2France
04 1India
05 5Italy
06 5Norway
07 1South Korea
08 1Spain
09 16Sweden
10 4Switzerland
11 45USA
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Regulatory Info : RX
Registration Country : USA
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
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Regulatory Info : RX
Registration Country : USA
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
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Regulatory Info : RX
Registration Country : USA
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
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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
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
