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01 14Taro Pharmaceutical Industries

02 1ANDA Repository

03 6Actavis Inc

04 3Adcock Ingram

05 24Alphapharm PTY Ltd

06 3Antibiotice SA

07 2Ascent Innovative Medicines

08 1Aurobindo Pharma Limited

09 6Bayer AG

10 1Belfar

11 1Bharat Parenterals Limited

12 2Bio Labs

13 1Chartwell Pharmaceuticals llc

14 1Chongqing Huapont Pharmaceutical

15 4Cosette Pharma

16 1Encube Ethicals

17 1Evolan Pharma AB

18 3Flagship Biotech International Pvt. Ltd

19 9Fougera Pharmaceuticals Inc.

20 1GLENMARK SPECLT

21 1Gia Nguyen Pharmaceutical

22 2Glenmark Pharmaceuticals

23 2Hikma Pharmaceuticals

24 1INTENDIS SpA

25 2Kolmar Korea Co., Ltd.

26 6Leo Pharma

27 1Lupin Ltd

28 1MC2 Therapeutics

29 6Merck & Co

30 4Organon

31 5Organon South Africa (Pty) Ltd

32 1PRODOTTI FORMENTI Srl

33 6Padagis

34 3Perrigo Company plc

35 2Pharmaderm

36 1Primus Pharmaceutical

37 1SHREE HARI INTL

38 3Savage Lab

39 1Seoul Pharma Co Ltd

40 1Smith & Kenner Pharmaceuticals

41 1Tanner Pharma

42 2Teva Pharmaceutical Industries

43 1Wellcopharma

44 1World Medicine

45 1Zhejiang Xianju Pharmaceutical Co. Ltd

46 1Zydus Lifesciences

47 1Zydus Pharmaceuticals

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PharmaCompass

01

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1987-06-17

Application Number : 71143

Regulatory Info : DISCN

Registration Country : USA

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02

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1988-08-24

Application Number : 72276

Regulatory Info : DISCN

Registration Country : USA

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03

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1992-04-30

Application Number : 73552

Regulatory Info : RX

Registration Country : USA

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04

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1994-09-15

Application Number : 74271

Regulatory Info : RX

Registration Country : USA

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05

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1994-09-30

Application Number : 74272

Regulatory Info : DISCN

Registration Country : USA

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06

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE

Brand Name : CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE;1%

Packaging :

Approval Date : 2001-05-29

Application Number : 75673

Regulatory Info : RX

Registration Country : USA

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07

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE

Brand Name : CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION;TOPICAL

Dosage Strength : EQ 0.05% BASE;1%

Packaging :

Approval Date : 2004-07-28

Application Number : 76493

Regulatory Info : RX

Registration Country : USA

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08

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : GEL, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 2003-12-02

Application Number : 76508

Regulatory Info : RX

Registration Country : USA

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09

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 2003-12-09

Application Number : 76543

Regulatory Info : RX

Registration Country : USA

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10

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : OINTMENT, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 2004-10-12

Application Number : 76753

Regulatory Info : RX

Registration Country : USA

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11

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 2007-05-21

Application Number : 77477

Regulatory Info : RX

Registration Country : USA

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12

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : SPRAY;TOPICAL

Dosage Strength : EQ 0.05% BASE/SPRAY

Packaging :

Approval Date : 2020-06-17

Application Number : 211722

Regulatory Info : DISCN

Registration Country : USA

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13

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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE

Brand Name : CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE

Dosage Form : SUSPENSION;TOPICAL

Dosage Strength : 0.064%;0.005%

Packaging :

Approval Date : 2020-09-02

Application Number : 213269

Regulatory Info : RX

Registration Country : USA

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14

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euroPLX 86 Munich
Not Confirmed

CALCIPOTRIOL (CALCIPOTRIOL MONOHYDRATE)

Brand Name : TARO-CALCIPOTRIOL / BETAMETHASONE GEL

Dosage Form : GEL

Dosage Strength : 50MCG/G

Packaging :

Approval Date :

Application Number : 2525178

Regulatory Info : Prescription

Registration Country : Canada

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15

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : DIPROSONE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 17536

Regulatory Info : DISCN

Registration Country : USA

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16

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : DIPROSONE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 17691

Regulatory Info : DISCN

Registration Country : USA

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17

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : DIPROSONE

Dosage Form : LOTION;TOPICAL

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

Packaging :

Approval Date : 1982-01-01

Application Number : 17781

Regulatory Info : DISCN

Registration Country : USA

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18

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : DIPROSONE

Dosage Form : DISC;TOPICAL

Dosage Strength : EQ 0.1% BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 17829

Regulatory Info : DISCN

Registration Country : USA

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19

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE

Brand Name : DIPROLENE

Dosage Form : OINTMENT, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 1983-07-27

Application Number : 18741

Regulatory Info : RX

Registration Country : USA

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20

euroPLX 86 Munich
Not Confirmed
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euroPLX 86 Munich
Not Confirmed

BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE

Brand Name : LOTRISONE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE;1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1984-07-10

Application Number : 18827

Regulatory Info : DISCN

Registration Country : USA

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