FDA APPLICATION 21656 | FDA Orange Book | Approved Drug Product List | PharmaCompass.com

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Product List 2022

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DIGITAL CONTENT

1 CORPORATE CONTENT #SupplierSpotlight, 12 DATA COMPILATION #PharmaFlow, 2655 NEWS #PharmaBuzz

1 CORPORATE CONTENT #SupplierSpotlight
12 DATA COMPILATION #PharmaFlow
2655 NEWS #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

13 All APIs, 7 USDMF, 6 CEP/COS, 7 KDMF, 7 NDC API, 8 Listed APIs

13 All APIs
7 USDMF
6 CEP/COS
7 KDMF
7 NDC API
8 Listed APIs

DEVELOPMENTS

306 Drugs in Development

306 Drugs in Development

FINISHED DOSAGE FORMULATIONS

832 FDF Dossiers, 287 FDA Orange Book, 148 Europe, 132 Canada, 202 Australia, 63 South Africa

832 FDF Dossiers
287 FDA Orange Book
148 Europe
132 Canada
202 Australia
63 South Africa

INSPECTIONS & REGISTRATIONS

96 FDA, 39 EDQM, 2 GDUFA

96 FDA
39 EDQM
2 GDUFA

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filter Applicant Reset all filters

2 All

01 2ABBVIE

filter Dosage Reset all filters

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01 2TABLET;ORAL

filter Regulatory Info Reset all filters

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01 2DISCN

filter Brand Name Reset all filters

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01 2TRICOR

filter RLD Reset all filters

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01 2Yes

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Brand Name : TRICOR

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RLD : Yes

TE Code :

FENOFIBRATE

Dosage Form : TABLET; ORAL

Proprietary Name : TRICOR

Dosage Strength : 48MG

Approval Date : 2004-11-05

Application Number : 21656

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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Brand Name : TRICOR

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RLD : Yes

TE Code :

FENOFIBRATE

Dosage Form : TABLET; ORAL

Proprietary Name : TRICOR

Dosage Strength : 145MG

Approval Date : 2004-11-05

Application Number : 21656

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

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