01 2ABRAXIS PHARM
02 1ANI PHARMS
03 8ASTRAZENECA
04 1AZURITY
05 5BAUSCH
06 3BIOVAIL
07 2ENDO OPERATIONS
08 6HIKMA INTL PHARMS
09 1I3 PHARMS
10 1IMPAX LABS INC
11 1INGENUS PHARMS LLC
12 1LEDERLE
13 1ORGANON USA INC
14 5PH HEALTH
15 5RUBICON
16 5SANDOZ
17 1SUN PHARM INDS INC
18 7SUN PHARM INDUSTRIES
19 2SUPERPHARM
20 1TEVA
21 1UBI
22 2WATSON LABS
23 1WATSON LABS TEVA
24 2WYETH AYERST
25 5ZYDUS LIFESCIENCES
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 1CAPSULE;ORAL
03 3INJECTABLE;INJECTION
04 1POWDER;INTRAVENOUS
05 2TABLET, CHEWABLE;ORAL
06 3TABLET, EXTENDED RELEASE;ORAL
07 43TABLET;ORAL
08 14TABLET;SUBLINGUAL
01 42DISCN
02 28RX
01 1BIDIL
02 1DILATRATE-SR
03 10ISORDIL
04 41ISOSORBIDE DINITRATE
05 2ISOSORBIDE DINITRATE AND HYDRALAZINE HYDROCHLORIDE
06 1METHYLPREDNISOLONE
07 2METHYLPREDNISOLONE SODIUM SUCCINATE
08 1PHENTERMINE HYDROCHLORIDE
09 1PROBENECID
10 8SORBITRATE
11 1THEO-24
12 1VORICONAZOLE
01 60No
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
