01 6Actavis Inc
02 3Adcock Ingram
03 24Alphapharm PTY Ltd
04 3Antibiotice
05 2Ascent Innovative Medicines
06 1Aurobindo Pharma Limited
07 6Bayer AG
08 1Belfar
09 1Bharat Parenterals Limited
10 2Bio Labs
11 2Chartwell Pharmaceuticals llc
12 1Chongqing Huapont Pharmaceutical
13 4Cosette Pharma
14 1DEEF Pharmaceutical
15 1Encube Ethicals
16 1Evolan Pharma AB
17 3Flagship Biotech International Pvt. Ltd
18 9Fougera Pharmaceuticals Inc.
19 1Gia Nguyen Pharmaceutical
20 3Glenmark Pharmaceuticals
21 2Hikma Pharmaceuticals
22 1INTENDIS SpA
23 2Kolmar Korea Co., Ltd.
24 6Leo Pharma
25 1Lupin Ltd
26 1MC2 Therapeutics
27 6Merck & Co
28 4Organon
29 5Organon South Africa (Pty) Ltd
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 14Taro Pharmaceutical Industries
40 2Teva Pharmaceutical Industries
41 1Trupharma
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 1Lotion
20 5OIN
21 2OINTMENT
22 7OINTMENT, AUGMENTED;TOPICAL
23 14OINTMENT;TOPICAL
24 3Ointment
25 2SPRAY;TOPICAL
26 1SUSPENSION FOR INJECTION
27 5SUSPENSION;TOPICAL
28 14cream
29 12ointment
30 2Blank
01 36DISCN
02 9Generic
03 6Originator
04 42RX
05 51Blank
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 1Defosalic
18 3Diproderm
19 1Diprogenta
20 1Diprolen
21 1Diprosalic
22 1Diprosalic Lotion
23 13Diprosone
24 1Diprosone Injection
25 1Diprotit
26 3Dovobet
27 1Dovobet Gel
28 1EKARZIN® 0.5 mg/g
29 2ENSTILAR
30 12Eleuphrat
31 1GENTRIDERM
32 2LOTRISONE
33 1Lotriderm Cream
34 1SAL-EKARZIN®
35 1SERNIVO
36 1SERTOSPAN
37 3TACLONEX
38 1TARO-CALCIPOTRIOL / BETAMETHASONE GEL
39 1Tinfozol
40 1Token
41 1WYNZORA
42 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 1United Kingdom
17 1Vietnam
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 : 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
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
