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01 1DR REDDYS LABS INC

02 1TARO

03 1BRECKENRIDGE PHARM

04 1ANDRX PHARM

05 1AUROBINDO PHARMA

06 1CHARTWELL

07 1CIPLA

08 1EMED MEDCL

09 1GEDEON RICHTER USA

10 1GLENMARK PHARMS LTD

11 1HERITAGE PHARMA AVET

12 1INVAGEN PHARMS

13 4KARO HLTHCARE

14 1MYLAN

15 1NATCO PHARMA

16 4NOVARTIS

17 1ORBION PHARMS

18 1ROXANE

19 1WOCKHARDT

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

RLD : No

TE Code : AB

TERBINAFINE HYDROCHLORIDE

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

Dr Reddy Company Banner

02

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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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

Breckenridge Pharmaceutical

03

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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : CREAM;TOPICAL

Dosage Strength : 1%

Approval Date : 2007-07-02

Application Number : 77511

RX/OTC/DISCN : OTC

RLD : No

TE Code :

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

TERBINAFINE HYDROCHLORIDE

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 :

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