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01 3Taro Pharmaceutical Industries

02 1Strides Pharma Science

03 3Alphapharm PTY Ltd

04 4Apotex Inc

05 3Bausch & Lomb Incorporated

06 3Bausch Health

07 2Chongqing Huapont Pharmaceutical

08 1Cosette Pharma

09 1DIFA COOPER SpA

10 1Difa Cooper

11 1Encube Ethicals

12 1Fougera Pharmaceuticals Inc.

13 1GRACEWAY

14 2Glenmark Pharmaceuticals

15 2Indoco Remedies Limited

16 1MEDA A.B.

17 4Meda AB

18 1Padagis

19 3Viatris

20 1Yangtze River Pharmaceutical Group

21 7iNova Pharmaceuticals

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : DISCN

Registration Country : USA

IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2014-06-24

Application Number : 202002

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

02

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Not Confirmed

IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2011-04-15

Application Number : 200173

Regulatory Info : RX

Registration Country : USA

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03

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Not Confirmed

IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 3.75%

Packaging :

Approval Date : 2021-01-26

Application Number : 205971

Regulatory Info : RX

Registration Country : USA

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04

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Not Confirmed

IMIQUIMOD

Brand Name : TARO-IMIQUIMOD PUMP

Dosage Form : CREAM

Dosage Strength : 5%/W/W

Packaging :

Approval Date :

Application Number : 2482983

Regulatory Info : Prescription

Registration Country : Canada

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05

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2012-04-06

Application Number : 91308

Regulatory Info : RX

Registration Country : USA

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06

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : ALDARA

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1997-02-27

Application Number : 20723

Regulatory Info : DISCN

Registration Country : USA

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07

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : ZYCLARA

Dosage Form : CREAM;TOPICAL

Dosage Strength : 3.75%

Packaging :

Approval Date : 2010-03-25

Application Number : 22483

Regulatory Info : RX

Registration Country : USA

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08

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : ZYCLARA

Dosage Form : CREAM;TOPICAL

Dosage Strength : 2.5%

Packaging :

Approval Date : 2011-07-15

Application Number : 22483

Regulatory Info : RX

Registration Country : USA

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09

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : ALDARA P

Dosage Form : CREAM

Dosage Strength : 5%

Packaging : 12X250MG/24X250MG

Approval Date :

Application Number : 2239505

Regulatory Info : Prescription

Registration Country : Canada

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10

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name :

Dosage Form : Cream

Dosage Strength : 5%

Packaging : 0.25g

Approval Date :

Application Number :

Regulatory Info :

Registration Country : China

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11

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name :

Dosage Form : Cream

Dosage Strength : 5%

Packaging : 3g

Approval Date :

Application Number :

Regulatory Info :

Registration Country : China

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12

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2011-04-18

Application Number : 200481

Regulatory Info : DISCN

Registration Country : USA

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13

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name : IMMUNOCARE

Dosage Form : Cream

Dosage Strength : 0.05

Packaging : 12 UNITS 250 MG 5% - DERMATOLOGICAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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14

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2011-02-28

Application Number : 91044

Regulatory Info : DISCN

Registration Country : USA

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15

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2010-02-25

Application Number : 78548

Regulatory Info : RX

Registration Country : USA

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16

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2012-03-06

Application Number : 201994

Regulatory Info : RX

Registration Country : USA

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17

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name :

Dosage Form : Cream

Dosage Strength : 3.75%

Packaging :

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : India

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18

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name :

Dosage Form : Cream

Dosage Strength : 5%

Packaging :

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : India

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19

Fi Europe 2024
Not Confirmed
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IMIQUIMOD

Brand Name : IMIQUIMOD

Dosage Form : CREAM;TOPICAL

Dosage Strength : 5%

Packaging :

Approval Date : 2010-09-07

Application Number : 78837

Regulatory Info : RX

Registration Country : USA

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20

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name : ALDARA

Dosage Form : Cream

Dosage Strength : 0.05

Packaging : 12 UNITS 250 MG 5% - DERMATOLOGICAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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21

Fi Europe 2024
Not Confirmed
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Imiquimodum

Brand Name : Aldara

Dosage Form : Cream

Dosage Strength : 5%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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22

Fi Europe 2024
Not Confirmed
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Imiquimodum

Brand Name : Zyclara

Dosage Form : Cream

Dosage Strength : 37.5mg/g

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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23

Fi Europe 2024
Not Confirmed
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Imiquimod

Brand Name :

Dosage Form : Cream

Dosage Strength : 100MG

Packaging : 2g:100mgx2tubes

Approval Date :

Application Number :

Regulatory Info :

Registration Country : China

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24

GRACEWAY

Country
Fi Europe 2024
Not Confirmed
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GRACEWAY

Country
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Fi Europe 2024
Not Confirmed

IMIQUIMOD

Brand Name : ZYCLARA

Dosage Form : CREAM; TOPICAL

Dosage Strength : 3.75%

Packaging :

Approval Date :

Application Number : 201153

Regulatory Info :

Registration Country : USA

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25

Meda AB

Country
Fi Europe 2024
Not Confirmed
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Meda AB

Country
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Fi Europe 2024
Not Confirmed

imiquimod

Brand Name : ALDARA

Dosage Form : CREAM

Dosage Strength : 5%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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26

Meda AB

Country
Fi Europe 2024
Not Confirmed
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Meda AB

Country
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Fi Europe 2024
Not Confirmed

imiquimod

Brand Name : Zyclara

Dosage Form : CREAM

Dosage Strength : 3.75%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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27

DIFA COOPER SpA

Country
Fi Europe 2024
Not Confirmed
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DIFA COOPER SpA

Country
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Fi Europe 2024
Not Confirmed

Imiquimod

Brand Name : Unocare

Dosage Form : Imiquimod 5% 250Mg 12 Units Cream Dermatological Use

Dosage Strength : cream derm 12 bust 250 mg 5%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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28

MEDA A.B.

Country
Fi Europe 2024
Not Confirmed
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MEDA A.B.

Country
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Fi Europe 2024
Not Confirmed

Imiquimod

Brand Name : Aldara Cream

Dosage Form : Imiquimod 5% 250Mg 12 Units Cream Dermatological Use

Dosage Strength : derm 12 sachets 250 mg 5%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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29

Meda AB

Country
Fi Europe 2024
Not Confirmed
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Meda AB

Country
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Fi Europe 2024
Not Confirmed

Imiquimod

Brand Name : Aldara

Dosage Form : Cream

Dosage Strength : 5%

Packaging : Disposable Bag

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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30

Meda AB

Country
Fi Europe 2024
Not Confirmed
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Meda AB

Country
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Fi Europe 2024
Not Confirmed

Imiquimod

Brand Name : Zyclara

Dosage Form : Cream

Dosage Strength : 3.75% w/w

Packaging : Disposable Bag

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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