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

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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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01 1Oral Drops
02 11TABLET
03 45TABLET;ORAL
04 25Tablet
05 5Blank
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01 4Allowed
02 1Authorized
03 6DISCN
04 1Generic Reference drug
05 3Marketed
06 2Not Marketed
07 23Prescription
08 39RX
09 8Blank
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01 2APO-MIDODRINE
02 2Augermite
03 6Gutron
04 10Hypotron
05 2JAMP MIDODRINE
06 2M-MIDODRINE
07 2MAR-MIDODRINE
08 2MIDODRINE
09 39MIDODRINE HYDROCHLORIDE
10 1Midodrin Leman
11 2Midodrin "Zentiva"
12 1Midodrina A.
13 1Midodrine Leman
14 2Midodrine "Medical Valley"
15 2Midodrine "Tillomed"
16 1Midron
17 3ORVATEN
18 3PROAMATINE
19 1Xerotil
20 3Blank
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01 10Canada
02 13Denmark
03 2France
04 1India
05 5Italy
06 5Norway
07 1South Korea
08 1Spain
09 4Switzerland
10 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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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 : 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
