FDA APPLICATION 19183 | 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 2022

Product List 2022

DIGITAL CONTENT

1 CORPORATE CONTENT #SupplierSpotlight, 11 DATA COMPILATION #PharmaFlow, 2675 NEWS #PharmaBuzz

1 CORPORATE CONTENT #SupplierSpotlight
11 DATA COMPILATION #PharmaFlow
2675 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

317 Drugs in Development

317 Drugs in Development

FINISHED DOSAGE FORMULATIONS

838 FDF Dossiers, 289 FDA Orange Book, 148 Europe, 132 Canada, 208 Australia, 61 South Africa

838 FDF Dossiers
289 FDA Orange Book
148 Europe
132 Canada
208 Australia
61 South Africa

INSPECTIONS & REGISTRATIONS

96 FDA, 39 EDQM, 2 GDUFA

96 FDA
39 EDQM
2 GDUFA

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01 1ABBVIE

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01 1SUSPENSION;ORAL

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01 1RX

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01 1CARAFATE

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01 1Yes

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Brand Name : CARAFATE

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RLD : Yes

TE Code : AB

Dosage Form : SUSPENSION; ORAL

Proprietary Name : CARAFATE

Dosage Strength : 1GM/10ML

Approval Date : 1993-12-16

Application Number : 19183

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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