01 1ANI PHARMS
02 9ASTRAZENECA
03 1AZURITY
04 5BAUSCH
05 3BIOVAIL
06 1ENDO OPERATIONS
07 6HIKMA INTL PHARMS
08 1I3 PHARMS
09 1IMPAX LABS INC
10 5PH HEALTH
11 1RICONPHARMA LLC
12 5RUBICON
13 5SANDOZ
14 1SUN PHARM INDS INC
15 7SUN PHARM INDUSTRIES
16 3SUPERPHARM
17 2WATSON LABS
18 1WATSON LABS TEVA
19 2WYETH AYERST
20 5ZYDUS LIFESCIENCES
01 2CAPSULE, EXTENDED RELEASE;ORAL
02 2TABLET, CHEWABLE;ORAL
03 3TABLET, EXTENDED RELEASE;ORAL
04 44TABLET;ORAL
05 14TABLET;SUBLINGUAL
01 39DISCN
02 26RX
01 1BIDIL
02 1DILATRATE-SR
03 10ISORDIL
04 42ISOSORBIDE DINITRATE
05 2ISOSORBIDE DINITRATE AND HYDRALAZINE HYDROCHLORIDE
06 9SORBITRATE
01 55No
02 10Yes
RLD : Yes
TE Code : AB
Brand Name : ISORDIL
Dosage Form : TABLET;ORAL
Dosage Strength : 40MG
Approval Date : 1988-07-29
Application Number : 12093
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-07-29
Application Number : 12093
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET;ORAL
Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-07-29
Application Number : 12093
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-07-29
Application Number : 12093
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : ISORDIL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1988-07-29
Application Number : 12093
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET;SUBLINGUAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-07-29
Application Number : 12940
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET;SUBLINGUAL
Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-07-29
Application Number : 12940
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET;SUBLINGUAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-07-29
Application Number : 12940
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : ISORDIL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 40MG
Approval Date : 1988-07-29
Application Number : 12882
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ISORDIL
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 40MG
Approval Date : 1988-07-29
Application Number : 12882
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
