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01 2BAUSCH

02 3COSETTE

03 1ENCUBE

04 2FOUGERA PHARMS

05 1MAYNE PHARMA

06 1MICAL PHARMS

07 4PADAGIS ISRAEL

08 1PERRIGO ISRAEL

09 1QUAGEN

10 2SUN PHARM INDS INC

11 2TARO

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PharmaCompass

01

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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

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02

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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 :

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03

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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 :

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04

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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

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05

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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

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06

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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

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07

PharmaVenue
Not Confirmed
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PharmaVenue
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**

Approval Date : 1990-12-27

Application Number : 19967

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

PharmaVenue
Not Confirmed
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PharmaVenue
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**

Approval Date : 1990-12-17

Application Number : 19968

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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

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10

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

HALOBETASOL PROPIONATE

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

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