01 1ANDA Repository
02 6Actavis Inc
03 3Adcock Ingram
04 24Alphapharm PTY Ltd
05 3Antibiotice SA
06 2Ascent Innovative Medicines
07 1Aurobindo Pharma Limited
08 6Bayer AG
09 1Belfar
10 1Bharat Parenterals Limited
11 2Bio Labs
12 1Chartwell Pharmaceuticals llc
13 1Chongqing Huapont Pharmaceutical
14 4Cosette Pharma
15 1Encube Ethicals
16 1Evolan Pharma AB
17 3Flagship Biotech International Pvt. Ltd
18 9Fougera Pharmaceuticals Inc.
19 1GLENMARK SPECLT
20 1Gia Nguyen Pharmaceutical
21 2Glenmark Pharmaceuticals
22 2Hikma Pharmaceuticals
23 1INTENDIS SpA
24 2Kolmar Korea Co., Ltd.
25 6Leo Pharma
26 1Lupin Ltd
27 1MC2 Therapeutics
28 11Merck & Co
29 4Organon
30 1PRODOTTI FORMENTI Srl
31 6Padagis
32 3Perrigo Company plc
33 2Pharmaderm
34 1Primus Pharmaceutical
35 1SHREE HARI INTL
36 3Savage Lab
37 1Seoul Pharma Co Ltd
38 1Smith & Kenner Pharmaceuticals
39 1Tanner Pharma
40 14Taro Pharmaceutical Industries
41 2Teva Pharmaceutical Industries
42 1Wellcopharma
43 1World Medicine
44 1Zhejiang Xianju Pharmaceutical Co. Ltd
45 1Zydus Lifesciences
46 1Zydus Pharmaceuticals
01 1AEROSOL, FOAM
02 2AEROSOL, FOAM;TOPICAL
03 1CRE
04 2CREAM
05 7CREAM, AUGMENTED;TOPICAL
06 18CREAM;TOPICAL
07 1CUTANEOUS SOLUTION
08 11Cream
09 1DISC;TOPICAL
10 1EAR DROPS, SOLUTION
11 1Ear drops, solution
12 4GEL
13 3GEL, AUGMENTED;TOPICAL
14 1Gel
15 1INJ
16 1LOT
17 5LOTION, AUGMENTED;TOPICAL
18 15LOTION;TOPICAL
19 5OIN
20 2OINTMENT
21 7OINTMENT, AUGMENTED;TOPICAL
22 14OINTMENT;TOPICAL
23 3Ointment
24 2SPRAY;TOPICAL
25 1SUSPENSION FOR INJECTION
26 5SUSPENSION;TOPICAL
27 14cream
28 12ointment
29 2Blank
01 35DISCN
02 9Generic
03 6Originator
04 43RX
05 50Blank
01 3ALPHATREX
02 47BETAMETHASONE DIPROPIONATE
03 1Baribit
04 1Betacortazol
05 1Biosone-SA
06 5CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE
07 1CALCIPOTRIENE AND BETHAMETHASONE DIPROPIONATE
08 1CLO-EKARZIN®
09 6CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE
10 1Calmio Gel
11 1Calmio Ointmentment
12 1Caneform
13 4DIPROLENE
14 1DIPROLENE AF
15 4DIPROSONE
16 1DOVOBET GEL
17 3Diproderm
18 1Diprogenta
19 1Diprolen
20 1Diprosalic
21 1Diprosalic Lotion
22 13Diprosone
23 1Diprosone Injection
24 1Diprotit
25 3Dovobet
26 1Dovobet Gel
27 1EKARZIN® 0.5 mg/g
28 2ENSTILAR
29 12Eleuphrat
30 1GENTRIDERM
31 2LOTRISONE
32 1Lotriderm Cream
33 1SAL-EKARZIN®
34 1SERNIVO
35 1SERTOSPAN
36 3TACLONEX
37 1TARO-CALCIPOTRIOL / BETAMETHASONE GEL
38 1Tinfozol
39 1Token
40 1WYNZORA
41 9Blank
01 24Australia
02 1Brazil
03 3Canada
04 2China
05 1Guatemala
06 7India
07 2Italy
08 1Norway
09 2Pakistan
10 3Romania
11 9South Africa
12 3South Korea
13 4Sweden
14 1Turkey
15 79USA
16 1Vietnam
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1985-07-31
Application Number : 70281
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1987-02-03
Application Number : 70885
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1987-02-03
Application Number : 71012
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1987-02-03
Application Number : 71085
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DIPROLENE
Dosage Form : CREAM, AUGMENTED;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1986-01-31
Application Number : 19408
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DIPROLENE
Dosage Form : GEL, AUGMENTED;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1991-11-22
Application Number : 19408
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1987-08-10
Application Number : 71467
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-06-26
Application Number : 19137
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-09-04
Application Number : 19141
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1985-08-12
Application Number : 70275
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE
Brand Name : TACLONEX
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.064%;0.005%
Packaging :
Approval Date : 2006-01-09
Application Number : 21852
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE
Brand Name : TACLONEX
Dosage Form : SUSPENSION;TOPICAL
Dosage Strength : 0.064%;0.005%
Packaging :
Approval Date : 2008-05-09
Application Number : 22185
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE HYDRATE
Brand Name : TACLONEX
Dosage Form : SUSPENSION;TOPICAL
Dosage Strength : 0.064%;0.005%
Packaging :
Approval Date :
Application Number : 22185
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
Brand Name : LOTRISONE
Dosage Form : LOTION;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 : 2000-12-08
Application Number : 20010
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DIPROLENE AF
Dosage Form : CREAM, AUGMENTED;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 : 1987-04-27
Application Number : 19555
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DIPROLENE
Dosage Form : LOTION, AUGMENTED;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 : 1988-08-01
Application Number : 19716
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-06-26
Application Number : 19136
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-09-04
Application Number : 19140
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALPHATREX
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-06-26
Application Number : 19138
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALPHATREX
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-09-04
Application Number : 19143
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALPHATREX
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1985-08-12
Application Number : 70273
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1987-08-10
Application Number : 71476
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1985-08-12
Application Number : 70274
Regulatory Info : DISCN
Registration Country : USA
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