01 1Ascent Innovative Medicines
02 2Bausch & Lomb Incorporated
03 4Bausch Health
04 3Cosette Pharma
05 1Encube Ethicals
06 2Fougera Pharmaceuticals Inc.
07 1Gujarat Pharma Lab
08 1MICAL PHARMS
09 1Mayne Pharma
10 4Padagis
11 1Perrigo Company plc
12 1Quagen Pharma
13 2Sun Pharmaceutical Industries Limited
14 2Taro Pharmaceutical Industries
01 2AEROSOL, FOAM;TOPICAL
02 1CREAM
03 5CREAM;TOPICAL
04 1Cream, Ointment
05 2LOTION
06 4LOTION;TOPICAL
07 1OINTMENT
08 8OINTMENT;TOPICAL
09 1Ointment
10 1UNKNOWN
01 7DISCN
02 4Prescription
03 12RX
04 3Blank
01 2BRYHALI
02 2DUOBRII
03 14HALOBETASOL PROPIONATE
04 1Helogen-6
05 1LEXETTE
06 5ULTRAVATE
07 1Blank
01 4Canada
02 2India
03 20USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Cream, Ointment
Dosage Strength : 0.05%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
HALOBETASOL PROPIONATE; TAZAROTENE
Brand Name : DUOBRII
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.01%;0.045%
Packaging :
Approval Date : 2019-04-25
Application Number : 209354
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BRYHALI
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.01%
Packaging :
Approval Date : 2018-11-06
Application Number : 209355
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : ULTRAVATE
Dosage Form : CREAM
Dosage Strength : 0.05%/W/W
Packaging : 15G/50G
Approval Date :
Application Number : 1962701
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : ULTRAVATE
Dosage Form : OINTMENT
Dosage Strength : 0.05%/W/W
Packaging : 15/50G
Approval Date :
Application Number : 1962728
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : BRYHALI
Dosage Form : LOTION
Dosage Strength : 0.01%/W/W
Packaging :
Approval Date :
Application Number : 2506262
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : DUOBRII
Dosage Form : LOTION
Dosage Strength : 0.01%/W/W
Packaging :
Approval Date :
Application Number : 2499967
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2005-06-14
Application Number : 77109
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2006-09-07
Application Number : 77721
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2007-04-24
Application Number : 78162
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2018-03-20
Application Number : 209978
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2004-12-16
Application Number : 76903
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2004-12-16
Application Number : 77001
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : Helogen-6
Dosage Form : Ointment
Dosage Strength : 0.5MG; 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : LEXETTE
Dosage Form : AEROSOL, FOAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2018-05-24
Application Number : 210566
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2004-12-16
Application Number : 76872
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2004-12-16
Application Number : 77123
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2020-06-03
Application Number : 211464
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : AEROSOL, FOAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2023-08-11
Application Number : 215266
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : UNKNOWN
Dosage Strength : UNKNOWN
Packaging :
Approval Date :
Application Number : 214285
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2020-10-06
Application Number : 213560
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1990-12-27
Application Number : 19967
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1990-12-17
Application Number : 19968
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2004-12-16
Application Number : 76994
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HALOBETASOL PROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2005-08-04
Application Number : 77227
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ULTRAVATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2015-11-06
Application Number : 208183
Regulatory Info : DISCN
Registration Country : USA
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