01 3ALEMBIC
02 3APOTEX
03 3AUROBINDO PHARMA LTD
04 3CHARTWELL RX
05 3ENDO OPERATIONS
06 3IMPAX PHARMS
07 3MANKIND PHARMA
08 3MYLAN PHARMS INC
09 3NOVUGEN
10 3RUBICON
11 3TAKEDA PHARMS USA
12 3THINQ PHARM-CRO PVT
13 3UPSHER SMITH LABS
14 3XIROMED
15 3ZYDUS LIFESCIENCES
01 45TABLET;ORAL
01 6DISCN
02 39RX
01 39MIDODRINE HYDROCHLORIDE
02 3ORVATEN
03 3PROAMATINE
01 42No
02 3Yes
RLD : No
TE Code :
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Approval Date : 2003-09-11
Application Number : 76514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2003-09-11
Application Number : 76514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 2004-07-02
Application Number : 76514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Approval Date : 2004-05-27
Application Number : 76449
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2004-05-27
Application Number : 76449
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 2005-12-16
Application Number : 76449
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
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Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-09-06
Application Number : 19815
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-09-06
Application Number : 19815
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2002-03-20
Application Number : 19815
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : MIDODRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Approval Date : 2003-09-10
Application Number : 76577
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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