01 5ACTAVIS MID ATLANTIC
02 1ALPHARMA US PHARMS
03 1ANDA REPOSITORY
04 1AUROBINDO PHARMA LTD
05 1CHARTWELL RX
06 4COSETTE
07 1ENCUBE
08 7FOUGERA PHARMS
09 2FOUGERA PHARMS INC
10 1GLENMARK PHARMS INC
11 1GLENMARK PHARMS LTD
12 1GLENMARK SPECLT
13 2HIKMA
14 4LEO PHARMA AS
15 1LUPIN LTD
16 1MC2
17 1MERCK SHARP DOHME
18 4ORGANON
19 4PADAGIS ISRAEL
20 2PADAGIS US
21 3PERRIGO NEW YORK
22 2PHARMADERM
23 1PRIMUS PHARMS
24 3SAVAGE LABS
25 6SCHERING
26 1SHREE HARI INTL
27 13TARO
28 1TASMAN PHARMA
29 2TEVA
30 1ZYDUS LIFESCIENCES
31 1ZYDUS PHARMS
01 2AEROSOL, FOAM;TOPICAL
02 7CREAM, AUGMENTED;TOPICAL
03 18CREAM;TOPICAL
04 1DISC;TOPICAL
05 3GEL, AUGMENTED;TOPICAL
06 5LOTION, AUGMENTED;TOPICAL
07 15LOTION;TOPICAL
08 7OINTMENT, AUGMENTED;TOPICAL
09 14OINTMENT;TOPICAL
10 2SPRAY;TOPICAL
11 5SUSPENSION;TOPICAL
01 34DISCN
02 44RX
03 1Blank
01 3ALPHATREX
02 47BETAMETHASONE DIPROPIONATE
03 5CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE
04 1CALCIPOTRIENE AND BETHAMETHASONE DIPROPIONATE
05 6CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE
06 4DIPROLENE
07 1DIPROLENE AF
08 4DIPROSONE
09 1ENSTILAR
10 2LOTRISONE
11 1SERNIVO
12 3TACLONEX
13 1WYNZORA
01 65No
02 13Yes
03 1Blank
RLD : No
TE Code :
Brand Name : DIPROSONE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1982-01-01
Application Number : 17536
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : DIPROSONE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1982-01-01
Application Number : 17691
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17781
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : DIPROSONE
Dosage Form : DISC;TOPICAL
Dosage Strength : EQ 0.1% BASE
Approval Date : 1982-01-01
Application Number : 17829
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1984-06-26
Application Number : 19137
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : DIPROLENE
Dosage Form : OINTMENT, AUGMENTED;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1983-07-27
Application Number : 18741
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
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**
Approval Date : 1984-07-10
Application Number : 18827
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1984-06-26
Application Number : 19136
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : BETAMETHASONE DIPROPIONATE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1984-09-04
Application Number : 19140
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ALPHATREX
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1984-06-26
Application Number : 19138
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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