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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 1Lacer

09 1Mayne Pharma

10 4Padagis

11 1Perrigo Company plc

12 1Quagen Pharma

13 2Sun Pharmaceutical Industries Limited

14 2Taro Pharmaceutical Industries

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PharmaCompass

01

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

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

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02

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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03

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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04

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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05

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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06

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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07

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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08

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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09

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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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10

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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11

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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12

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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13

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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14

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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15

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

Brand Name : HALOBETASOL PROPIONATE

Dosage Form : UNKNOWN

Dosage Strength : UNKNOWN

Packaging :

Approval Date :

Application Number : 214285

Regulatory Info :

Registration Country : USA

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16

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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17

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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18

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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19

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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20

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

HALOBETASOL PROPIONATE

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

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