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01 8ABBVIE

02 2DR REDDYS

03 2MANKIND PHARMA

04 5AJANTA PHARMA LTD

05 7ALEMBIC

06 4AMNEAL

07 3ANI PHARMS

08 2APOTEX

09 4AUROBINDO PHARMA

10 3AUROBINDO PHARMA LTD

11 2BAUSCH

12 4BOSTAL

13 3CHARTWELL

14 4CHARTWELL RX

15 3CIPHER PHARMS INC

16 2CIPLA

17 2CREEKWOOD PHARMS

18 3GLENMARK PHARMS LTD

19 2HETERO LABS LTD III

20 5IMPAX LABS

21 3INVAGEN PHARMS

22 2JAGOTEC

23 7LUPIN

24 2LUPIN LTD

25 4MACLEODS PHARMS LTD

26 3MYLAN

27 4MYLAN PHARMS INC

28 3NOVAST LABS

29 2PHARMOBEDIENT

30 2PRINSTON INC

31 3REYOUNG

32 5RHODES PHARMS

33 7RISING

34 2ROSEMONT

35 2SALIX

36 2SUN PHARM

37 5SUN PHARM INDS LTD

38 3TORRENT

39 2YICHANG HUMANWELL

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PharmaCompass

02

  • 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

FENOFIBRATE

Brand Name : FENOFIBRATE

Dosage Form : TABLET;ORAL

Dosage Strength : 54MG

Approval Date : 2019-09-06

Application Number : 210670

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

FENOFIBRATE

Brand Name : FENOFIBRATE

Dosage Form : TABLET;ORAL

Dosage Strength : 54MG

Approval Date : 2020-06-12

Application Number : 213864

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

04

FENOFIBRATE

Brand Name : TRICOR (MICRONIZED)

Dosage Form : CAPSULE;ORAL

Dosage Strength : 67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1998-02-09

Application Number : 19304

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

05

FENOFIBRATE

Brand Name : TRICOR (MICRONIZED)

Dosage Form : CAPSULE;ORAL

Dosage Strength : 134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1999-06-30

Application Number : 19304

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

06

FENOFIBRATE

Brand Name : TRICOR (MICRONIZED)

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1999-06-30

Application Number : 19304

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

07

FENOFIBRATE

Brand Name : TRICOR

Dosage Form : TABLET;ORAL

Dosage Strength : 54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2001-09-04

Application Number : 21203

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

08

FENOFIBRATE

Brand Name : TRICOR

Dosage Form : TABLET;ORAL

Dosage Strength : 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2001-09-04

Application Number : 21203

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

09

FENOFIBRATE

Brand Name : TRICOR

Dosage Form : TABLET;ORAL

Dosage Strength : 48MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2004-11-05

Application Number : 21656

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

10

FENOFIBRATE

Brand Name : TRICOR

Dosage Form : TABLET;ORAL

Dosage Strength : 145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2004-11-05

Application Number : 21656

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner