DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR REDDYS LABS INC
02 1BRECKENRIDGE PHARM
03 1ANDRX PHARM
04 1AUROBINDO PHARMA
05 1CHARTWELL
06 1CIPLA
07 1EMED MEDCL
08 1GEDEON RICHTER USA
09 1GLENMARK PHARMS LTD
10 1HERITAGE PHARMA AVET
11 1INVAGEN PHARMS
12 4KARO HLTHCARE
13 1MYLAN
14 1NATCO PHARMA
15 4NOVARTIS
16 1ORBION PHARMS
17 1ROXANE
18 1TARO
19 1WOCKHARDT
01 3CREAM;TOPICAL
02 2GRANULE;ORAL
03 2SOLUTION;TOPICAL
04 1SPRAY;TOPICAL
05 1TABLET; ORAL
06 16TABLET;ORAL
01 12DISCN
02 4OTC
03 8RX
04 1Blank
01 6LAMISIL
02 2LAMISIL AT
03 17TERBINAFINE HYDROCHLORIDE
01 18No
02 6Yes
03 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : TERBINAFINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 2007-07-02
Application Number : 76390
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : TERBINAFINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 2010-06-04
Application Number : 77714
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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Dosage Strength : 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
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