FDA APPLICATION 20945 | FDA Orange Book | Approved Drug Product List | PharmaCompass.com

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AbbVie Inc

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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

PRESENTATION(s)

Product List 2025

Product List 2025

DIGITAL CONTENT

1 Corporate Content #SupplierSpotlight, 14 Data Compilation #PharmaFlow, 2772 News #PharmaBuzz

1 Corporate Content #SupplierSpotlight
14 Data Compilation #PharmaFlow
2772 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

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

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

DEVELOPMENTS

1296 Drugs in Development

1296 Drugs in Development

FINISHED DOSAGE FORMULATIONS

1001 FDF Dossiers, 297 FDA Orange Book, 277 Europe, 130 Canada, 233 Australia, 64 South Africa

1001 FDF Dossiers
297 FDA Orange Book
277 Europe
130 Canada
233 Australia
64 South Africa

INSPECTIONS & REGISTRATIONS

94 FDA, 45 EDQM, 2 GDUFA

94 FDA
45 EDQM
2 GDUFA

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filter Applicant Reset all filters

1 All

01 1ABBVIE

filter Dosage Reset all filters

1 All

01 1CAPSULE;ORAL

filter Regulatory Info Reset all filters

1 All

01 1DISCN

filter Brand Name Reset all filters

1 All

01 1NORVIR

filter RLD Reset all filters

1 All

01 1Yes

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Brand Name : NORVIR

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RLD : Yes

TE Code :

Dosage Form : CAPSULE; ORAL

Proprietary Name : NORVIR

Dosage Strength : 100MG **Federal Register...

Approval Date : 1999-06-29

Application Number : 20945

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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