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01 1ANI Pharmaceuticals Inc

02 2Avondale Pharmaceutical

03 4Pfizer Inc

04 1Rising Pharmaceuticals Inc

05 1ScieGen Pharmaceuticals

06 3Taro Pharmaceutical Industries

07 1Teofarma

08 1The J. Molner Company

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PharmaCompass

01

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 2002-12-20

Application Number : 76263

Regulatory Info : DISCN

Registration Country : USA

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02

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 1998-03-30

Application Number : 75187

Regulatory Info : DISCN

Registration Country : USA

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03

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 1999-04-27

Application Number : 75374

Regulatory Info : RX

Registration Country : USA

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04

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : FLORONE

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Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1982-01-01

Application Number : 17741

Regulatory Info : DISCN

Registration Country : USA

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05

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : PSORCON E

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 1982-01-01

Application Number : 17994

Regulatory Info : DISCN

Registration Country : USA

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06

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : FLORONE E

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 1985-08-28

Application Number : 19259

Regulatory Info : DISCN

Registration Country : USA

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07

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : PSORCON

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 1985-08-28

Application Number : 19260

Regulatory Info : DISCN

Registration Country : USA

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08

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 2017-02-27

Application Number : 207440

Regulatory Info : RX

Registration Country : USA

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09

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 2015-07-24

Application Number : 206572

Regulatory Info : DISCN

Registration Country : USA

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10

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : PSORCON

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 : 1992-11-20

Application Number : 20205

Regulatory Info : DISCN

Registration Country : USA

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11

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 1999-05-14

Application Number : 75331

Regulatory Info : RX

Registration Country : USA

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12

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 2000-04-24

Application Number : 75508

Regulatory Info : RX

Registration Country : USA

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13

OPRD
Not Confirmed
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OPRD
Not Confirmed

Diflorasone Diacetate

Brand Name : Wall

Dosage Form : Gel

Dosage Strength : 0.5MG

Packaging :

Approval Date : 1984-12-01

Application Number : 56346

Regulatory Info : Cancelled

Registration Country : Spain

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14

OPRD
Not Confirmed
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OPRD
Not Confirmed

DIFLORASONE DIACETATE

Brand Name : DIFLORASONE DIACETATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 0.05%

Packaging :

Approval Date : 2018-06-12

Application Number : 210753

Regulatory Info : RX

Registration Country : USA

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