01 1BRECKENRIDGE PHARM
02 1ANDRX PHARM
03 1AUROBINDO PHARMA
04 1CHARTWELL
05 1CIPLA
06 1EMED MEDCL
07 1GEDEON RICHTER USA
08 1GLENMARK PHARMS LTD
09 1HERITAGE PHARMA AVET
10 1INVAGEN PHARMS
11 4KARO HLTHCARE
12 1MYLAN
13 1NATCO PHARMA
14 4NOVARTIS
15 1ORBION PHARMS
16 1ROXANE
17 1SENORES PHARMS
18 1TARO
19 1WOCKHARDT
01 3CREAM;TOPICAL
02 2GRANULE;ORAL
03 2SOLUTION;TOPICAL
04 1SPRAY;TOPICAL
05 1TABLET; ORAL
06 16TABLET;ORAL
01 13DISCN
02 4OTC
03 7RX
04 1Blank
01 6LAMISIL
02 2LAMISIL AT
03 17TERBINAFINE HYDROCHLORIDE
01 18No
02 6Yes
03 1Blank
RLD : No
TE Code :
Brand Name : TERBINAFINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 2010-06-04
Application Number : 77714
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : TERBINAFINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 2007-07-02
Application Number : 76377
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : LAMISIL
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 1%
Approval Date : 1997-10-17
Application Number : 20749
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : LAMISIL
Dosage Form : CREAM;TOPICAL
Dosage Strength : 1%
Approval Date : 1999-03-09
Application Number : 20980
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LAMISIL AT
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 1%
Approval Date : 2000-03-17
Application Number : 21124
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LAMISIL AT
Dosage Form : SPRAY;TOPICAL
Dosage Strength : 1%
Approval Date : 2000-03-17
Application Number : 21124
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : LAMISIL
Dosage Form : CREAM;TOPICAL
Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1992-12-30
Application Number : 20192
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : LAMISIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-05-10
Application Number : 20539
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LAMISIL
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 125MG BASE/PACKET
Approval Date : 2007-09-28
Application Number : 22071
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LAMISIL
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 187.5MG BASE/PACKET
Approval Date : 2007-09-28
Application Number : 22071
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
