FDA APPLICATION 21252 | FDA Orange Book | Approved Drug Product List | PharmaCompass.com

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EVENTS

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PRESENTATION(s)

Product List 2025

Product List 2025

DIGITAL CONTENT

1 Corporate Content #SupplierSpotlight, 14 Data Compilation #PharmaFlow, 2773 News #PharmaBuzz

1 Corporate Content #SupplierSpotlight
14 Data Compilation #PharmaFlow
2773 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

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

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

DEVELOPMENTS

1299 Drugs in Development

1299 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

2 All

01 2ABBVIE

filter Dosage Reset all filters

2 All

01 2SUPPOSITORY;RECTAL

filter Regulatory Info Reset all filters

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01 1DISCN

02 1RX

filter Brand Name Reset all filters

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01 2CANASA

filter RLD Reset all filters

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01 1No

02 1Yes

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Brand Name : CANASA

Florida Innovation

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RLD : Yes

TE Code : AB

Dosage Form : SUPPOSITORY; RECTAL

Proprietary Name : CANASA

Dosage Strength : 1GM

Approval Date : 2004-11-05

Application Number : 21252

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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Brand Name : CANASA

Florida Innovation

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RLD : No

TE Code :

Dosage Form : SUPPOSITORY; RECTAL

Proprietary Name : CANASA

Dosage Strength : 500MG

Approval Date : 2001-01-05

Application Number : 21252

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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