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
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 34DISCN
02 9Generic
03 6Originator
04 3Prescription
05 44RX
06 47Blank
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 : 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 : LOTION;TOPICAL
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1988-08-24
Application Number : 72276
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 : 1992-04-30
Application Number : 73552
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 : 1994-09-15
Application Number : 74271
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 : 1994-09-30
Application Number : 74272
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : Prescription
Registration Country : Canada
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
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 : 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
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