01 6SCHERING
02 5ACTAVIS MID ATLANTIC
03 1ALPHARMA US PHARMS
04 2AUROBINDO PHARMA LTD
05 1CHARTWELL MOLECULAR
06 1CHARTWELL RX
07 4COSETTE
08 1ENCUBE
09 7FOUGERA PHARMS
10 2FOUGERA PHARMS INC
11 1GLENMARK PHARMS
12 1GLENMARK PHARMS LTD
13 1GLENMARK SPECLT
14 2HIKMA
15 4LEO PHARMA AS
16 1LUPIN
17 1MC2
18 1MERCK SHARP DOHME
19 4ORGANON
20 4PADAGIS ISRAEL
21 2PADAGIS US
22 3PERRIGO NEW YORK
23 2PHARMADERM
24 1PRIMUS PHARMS
25 3SAVAGE LABS
26 1SHREE HARI INTL
27 12SUN PHARMA CANADA
28 1TARO
29 2TEVA
30 1TP ANDA HOLDINGS
31 1ZYDUS LIFESCIENCES
32 1ZYDUS PHARMS
01 2AEROSOL, FOAM;TOPICAL
02 7CREAM, AUGMENTED;TOPICAL
03 19CREAM;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 39DISCN
02 40RX
03 1Blank
01 3ALPHATREX
02 48BETAMETHASONE 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 66No
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Dosage Strength : EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : No
TE Code :
Brand Name : DIPROLENE
Dosage Form : CREAM, AUGMENTED;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1986-01-31
Application Number : 19408
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : DIPROLENE
Dosage Form : GEL, AUGMENTED;TOPICAL
Dosage Strength : EQ 0.05% BASE
Approval Date : 1991-11-22
Application Number : 19408
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 :
