01 2BAUSCH
02 3COSETTE
03 1ENCUBE
04 2FOUGERA PHARMS
05 1LACER PHARMA
06 1MAYNE PHARMA
07 4PADAGIS ISRAEL
08 1PERRIGO ISRAEL
09 1QUAGEN
10 2SUN PHARM INDS INC
11 2TARO
01 2AEROSOL, FOAM;TOPICAL
02 5CREAM;TOPICAL
03 4LOTION;TOPICAL
04 8OINTMENT;TOPICAL
05 1UNKNOWN
01 7DISCN
02 12RX
03 1Blank
01 1BRYHALI
02 1DUOBRII
03 14HALOBETASOL PROPIONATE
04 1LEXETTE
05 3ULTRAVATE
01 13No
02 6Yes
03 1Blank
RLD : No
TE Code : AB
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2005-06-14
Application Number : 77109
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2006-09-07
Application Number : 77721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2004-12-16
Application Number : 76903
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2004-12-16
Application Number : 77001
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2004-12-16
Application Number : 76872
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2004-12-16
Application Number : 77123
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ULTRAVATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1990-12-27
Application Number : 19967
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ULTRAVATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1990-12-17
Application Number : 19968
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2004-12-16
Application Number : 76994
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Approval Date : 2005-08-04
Application Number : 77227
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
