01 1ACTAVIS MID ATLANTIC
02 10BAYER HEALTHCARE LLC
03 3BAYER HLTHCARE
04 1BAYER PHARMS
05 3FOUGERA PHARMS
06 1GLENMARK PHARMS
07 1GLENMARK SPECLT
08 1HIKMA
09 1MERCK SHARP DOHME
10 1NOVITIUM PHARMA
11 1ORGANON
12 1P AND L
13 1PADAGIS US
14 1SCHERING
15 5SCHERING PLOUGH
16 1SCIEGEN PHARMS INC
17 6TARO
18 1TEVA
19 1TEVA PHARMS
20 1THINQ PHARM-CRO PVT
21 1TRUPHARMA
01 3CREAM, TABLET;TOPICAL, VAGINAL
02 10CREAM;TOPICAL
03 6CREAM;VAGINAL
04 1Cream; Topical
05 4LOTION;TOPICAL
06 1Lotion; Topical
07 7SOLUTION;TOPICAL
08 2Solution; Topical
09 5TABLET;VAGINAL
10 4TROCHE/LOZENGE;ORAL
01 19DISCN
02 3OTC
03 17RX
04 4Blank
01 13CLOTRIMAZOLE
02 6CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE
03 2GYNE-LOTRIMIN
04 2GYNE-LOTRIMIN 3
05 1GYNE-LOTRIMIN 3 COMBINATION PACK
06 1GYNE-LOTRIMIN COMBINATION PACK
07 1GYNIX
08 3LOTRIMIN
09 3LOTRIMIN AF
10 2LOTRISONE
11 4MYCELEX
12 2MYCELEX-7
13 1MYCELEX-7 COMBINATION PACK
14 1MYCELEX-G
15 1TRIVAGIZOLE 3
01 27No
02 12Yes
03 4Blank
RLD : Yes
TE Code :
Brand Name : GYNE-LOTRIMIN
Dosage Form : TABLET;VAGINAL
Dosage Strength : 100MG
Approval Date : 1990-11-30
Application Number : 17717
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : GYNE-LOTRIMIN
Dosage Form : CREAM;VAGINAL
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1990-11-30
Application Number : 18052
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : MYCELEX
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18181
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD :
TE Code :
Brand Name : MYCELEX
Dosage Form : Solution; Topical
Dosage Strength : 1%
Approval Date :
Application Number : 18181
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code :
Brand Name : MYCELEX-7
Dosage Form : TABLET;VAGINAL
Dosage Strength : 100MG
Approval Date : 1991-12-26
Application Number : 18182
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : MYCELEX
Dosage Form : CREAM;TOPICAL
Dosage Strength : 1%
Approval Date : 1982-01-01
Application Number : 18183
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : MYCELEX-7
Dosage Form : CREAM;VAGINAL
Dosage Strength : 1%
Approval Date : 1991-12-26
Application Number : 18230
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : MYCELEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1983-06-17
Application Number : 18713
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LOTRIMIN
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17613
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LOTRIMIN
Dosage Form : CREAM;TOPICAL
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17619
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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