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01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAthena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

RLD : Yes

TE Code :

FENOFIBRIC ACID

Brand Name : FIBRICOR

Dosage Form : TABLET;ORAL

Dosage Strength : 35MG

Approval Date : 2009-08-14

Application Number : 22418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Athena Company Banner

03

  • 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

04

  • 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

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAthena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

RLD : Yes

TE Code :

FENOFIBRIC ACID

Brand Name : FIBRICOR

Dosage Form : TABLET;ORAL

Dosage Strength : 105MG

Approval Date : 2009-08-14

Application Number : 22418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Athena Company Banner

06

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Dosage Strength : 67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

07

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Dosage Strength : 134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

08

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Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

09

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

10

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