Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 3Mankind Pharma
02 1Abacus Medicine
03 3Alembic Pharmaceuticals Limited
04 5Apotex Inc
05 2Aspire Pharma
06 3Aurobindo Pharma Limited
07 1BONISCONTRO & GAZZONE Srl
08 3Brancaster 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 2Medical Valley
21 1Myungmoon Pharm. Co., LTD.
22 3Novugen
23 3PH HEALTH
24 3Rubicon Research
25 2SANIS HEALTH INC
26 3Shijiazhuang Yiling Pharmaceutical Co.,Ltd.
27 1Smith & Kenner Pharmaceuticals
28 2Substipharm
29 3THINQ Pharma-CRO PVT Ltd
30 3Takeda Pharmaceutical
31 2Tillomed Laboratories Ltd
32 1UNION HEALTH Srl
33 3Viatris
34 3Xiromed
35 2Zentiva
36 3Zydus Lifesciences
01 1Oral Drops
02 11TABLET
03 45TABLET;ORAL
04 23Tablet
05 5Blank
01 4Allowed
02 16Approved
03 1Authorized
04 6DISCN
05 1Generic Reference drug
06 10Prescription
07 39RX
08 8Blank
01 2APO-MIDODRINE
02 2Augermid
03 6Gutron
04 3Hypotron
05 2JAMP MIDODRINE
06 2M-MIDODRINE
07 2MAR-MIDODRINE
08 2MIDODRINE
09 39MIDODRINE HYDROCHLORIDE
10 1Midodrin Abacus Medicine
11 1Midodrin Leman
12 1Midodrina A.
13 1Midodrine Ebb
14 2Midodrine Evolan
15 1Midodrine Leman
16 1Midodrine Medartuum
17 2Midodrine Medical Valley
18 2Midodrine Tillomed
19 2Midodrine Zentiva
20 1Midron
21 3ORVATEN
22 3PROAMATINE
23 1Xerotil
24 3Blank
01 10Canada
02 2France
03 1India
04 5Italy
05 1South Korea
06 1Spain
07 16Sweden
08 4Switzerland
09 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
