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01 1Rusan Pharma

02 1Breckenridge Pharmaceutical

03 1Octavius Pharma Pvt. Ltd

04 2Towa Pharmaceutical

05 1ANDRX LABS LLC

06 1Actavis Inc

07 1Activo Health

08 1Akriti Pharmaceuticals Pvt. Ltd.

09 1Alter Laboratories Sa

10 1Apotex Inc

11 2Associated Biotech

12 1Auro Pharma Inc

13 3Aurobindo Pharma Limited

14 1Aurovitas Spain, Sau

15 1Avet Pharmaceuticals

16 2Bio Labs

17 2Biofarma Pharmaceutical Industry and Commerce Inc

18 1Chartwell Pharmaceuticals llc

19 1Chongqing Huapont Pharmaceutical

20 1Cipla

21 2Combix Laboratories Slu

22 2DOC Generici

23 2EG SpA

24 1Emed Medical Company

25 1Fitopharm

26 1Flagship Biotech International Pvt. Ltd

27 6GSK

28 1Gedeon Richter

29 2Gia Nguyen Pharmaceutical

30 1Glenmark Pharmaceuticals

31 1Gujarat Pharma Lab

32 1InvaGen Pharmaceuticals Inc

33 4Karo Pharma

34 2Kolmar Korea Co., Ltd.

35 1LABORATORIOS NORMON SA

36 3LPB IST.FARMACEUTICO Srl

37 1Laboratorios Alter

38 1Loxim Industries

39 1Madras Pharmaceuticals

40 1Medius Ag

41 2Meracine

42 1Moberg Pharma

43 1Myungmoon Pharm. Co., LTD.

44 1NOVARTIS ANIMAL HEALTH CANADA INC

45 1Natco Pharma

46 4Nobel Ilac Sanayii Ve Ticaret A.S.

47 8Novartis Pharmaceuticals Corporation

48 1OrBion Pharmaceuticals

49 1PRO DOC LIMITEE

50 3Pharmascience Inc.

51 1ROXANE

52 1S.F.GROUP Srl

53 1SANIS HEALTH INC

54 1SIVEM PHARMACEUTICALS ULC

55 3Sandoz B2B

56 1Scholl

57 1Senores Pharmaceuticals

58 1Seoul Pharma Co Ltd

59 1TECNIGEN Srl

60 1Taro Pharmaceutical Industries

61 2Teva Pharmaceutical Industries

62 1Vaishali Pharma Ltd

63 3Viatris

64 1Wockhardt

65 1World Medicine

66 2ZRS LABS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothRusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

Regulatory Info :

Registration Country : India

Terbinafine Hydrochloride

Brand Name :

Dosage Form : Cream

Dosage Strength : 1%/w/v

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Rusan Pharma

02

TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2010-06-04

Application Number : 77714

Regulatory Info : DISCN

Registration Country : USA

Breckenridge Pharmaceutical

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOctavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.

Regulatory Info :

Registration Country : India

Terbinafine Hydrochloride

Brand Name : Terbinafine Hydrochloride

Dosage Form : Ointment

Dosage Strength : 1%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Authorized

Registration Country : Spain

Terbinafine Hydrochloride

Brand Name : Terbinafina Pensa

Dosage Form : Cream

Dosage Strength : 10MG

Packaging :

Approval Date : 2007-02-12

Application Number : 68462

Regulatory Info : Authorized

Registration Country : Spain

Towa Pharmaceutical

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Authorized

Registration Country : Spain

Terbinafine Hydrochloride

Brand Name : Terbinafina Pensa

Dosage Form : Tablet

Dosage Strength : 250MG

Packaging :

Approval Date : 2008-03-17

Application Number : 69684

Regulatory Info : Authorized

Registration Country : Spain

Towa Pharmaceutical

06

PackExpo
Not Confirmed
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TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET; ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date :

Application Number : 76713

Regulatory Info :

Registration Country : USA

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07

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2007-07-02

Application Number : 76377

Regulatory Info : DISCN

Registration Country : USA

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08

TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2007-07-02

Application Number : 77137

Regulatory Info : DISCN

Registration Country : USA

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09

PackExpo
Not Confirmed
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TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2007-07-02

Application Number : 77065

Regulatory Info : DISCN

Registration Country : USA

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10

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : LAMISIL

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 1%

Packaging :

Approval Date : 1997-10-17

Application Number : 20749

Regulatory Info : DISCN

Registration Country : USA

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11

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TERBINAFINE HYDROCHLORIDE

Brand Name : LAMISIL

Dosage Form : CREAM;TOPICAL

Dosage Strength : 1%

Packaging :

Approval Date : 1999-03-09

Application Number : 20980

Regulatory Info : OTC

Registration Country : USA

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12

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : LAMISIL AT

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 1%

Packaging :

Approval Date : 2000-03-17

Application Number : 21124

Regulatory Info : OTC

Registration Country : USA

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13

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TERBINAFINE HYDROCHLORIDE

Brand Name : LAMISIL AT

Dosage Form : SPRAY;TOPICAL

Dosage Strength : 1%

Packaging :

Approval Date : 2000-03-17

Application Number : 21124

Regulatory Info : OTC

Registration Country : USA

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14

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2007-07-02

Application Number : 77195

Regulatory Info : DISCN

Registration Country : USA

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15

PackExpo
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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**

Packaging :

Approval Date : 1992-12-30

Application Number : 20192

Regulatory Info : DISCN

Registration Country : USA

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16

PackExpo
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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**

Packaging :

Approval Date : 1996-05-10

Application Number : 20539

Regulatory Info : DISCN

Registration Country : USA

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17

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : LAMISIL

Dosage Form : GRANULE;ORAL

Dosage Strength : EQ 125MG BASE/PACKET

Packaging :

Approval Date : 2007-09-28

Application Number : 22071

Regulatory Info : DISCN

Registration Country : USA

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18

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : LAMISIL

Dosage Form : GRANULE;ORAL

Dosage Strength : EQ 187.5MG BASE/PACKET

Packaging :

Approval Date : 2007-09-28

Application Number : 22071

Regulatory Info : DISCN

Registration Country : USA

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19

PackExpo
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TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2007-07-02

Application Number : 76390

Regulatory Info : RX

Registration Country : USA

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20

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TERBINAFINE HYDROCHLORIDE

Brand Name : TERBINAFINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 2007-07-02

Application Number : 77136

Regulatory Info : DISCN

Registration Country : USA

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