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01 3ACTAVIS MID ATLANTIC

02 6ALEMBIC

03 3AMNEAL

04 1ANI PHARMS

05 1APOTEX

06 2AUROBINDO PHARMA USA

07 2BEACH PRODS

08 1CHARTWELL RX

09 3COSETTE

10 3ENCUBE

11 1EPIC PHARMA LLC

12 9FOUGERA PHARMS

13 1FOUGERA PHARMS INC

14 1GALDERMA LABS

15 2GALDERMA LABS LP

16 3GLENMARK PHARMS LTD

17 3GLENMARK SPECLT

18 1HARROW EYE

19 6HIKMA

20 3LUPIN LTD

21 3MACLEODS PHARMS LTD

22 1NOVAST LABS

23 2NOVEL LABS INC

24 3PADAGIS ISRAEL

25 2PADAGIS US

26 3PAI HOLDINGS PHARM

27 3PHARMOBEDIENT

28 1PRIMUS PHARMS

29 1PRINSTON INC

30 1QUAGEN

31 1RISING

32 1SAPTALIS PHARMS

33 1SCIEGEN PHARMS INC

34 11TARO

35 1TEVA PHARMS USA

36 2TORRENT

37 1WOCKHARDT BIO AG

38 2XIROMED

39 1ZYDUS LIFESCIENCES

40 3ZYDUS PHARMS

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PharmaCompass

01

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : TEMOVATE

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Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1985-12-27

Application Number : 19322

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : TEMOVATE

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Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1985-12-27

Application Number : 19323

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : TEMOVATE

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1990-02-22

Application Number : 19966

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : TEMOVATE

Dosage Form : GEL;TOPICAL

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

Approval Date : 1994-04-29

Application Number : 20337

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : TEMOVATE E

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 : 1994-06-17

Application Number : 20340

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : CLOBEX

Dosage Form : LOTION;TOPICAL

Dosage Strength : 0.05%

Approval Date : 2003-07-24

Application Number : 21535

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : CLOBEX

Dosage Form : SHAMPOO;TOPICAL

Dosage Strength : 0.05%

Approval Date : 2004-02-05

Application Number : 21644

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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08

Bio-Europe Autumn
Not Confirmed
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : CLOBEX

Dosage Form : SPRAY;TOPICAL

Dosage Strength : 0.05%

Approval Date : 2005-10-27

Application Number : 21835

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AT

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09

PHARMOBEDIENT

Country
Bio-Europe Autumn
Not Confirmed
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PHARMOBEDIENT

Country
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Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : OLUX

Dosage Form : AEROSOL, FOAM;TOPICAL

Dosage Strength : 0.05%

Approval Date : 2000-05-26

Application Number : 21142

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

PHARMOBEDIENT

Country
Bio-Europe Autumn
Not Confirmed
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PHARMOBEDIENT

Country
arrow
Bio-Europe Autumn
Not Confirmed

CLOBETASOL PROPIONATE

Brand Name : OLUX E

Dosage Form : AEROSOL, FOAM;TOPICAL

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

Approval Date : 2007-01-12

Application Number : 22013

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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