Sciegen Pharmaceuticals | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com

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ScieGen Pharmaceuticals
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ScieGen Pharmaceuticals

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INTERVIEW #SpeakPharma, VLOG #PharmaReel, DATA COMPILATION #PharmaFlow, 47 NEWS #PharmaBuzz

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FINISHED DOSAGE FORMULATIONS

219 FDF Dossiers, 219 FDA Orange Book

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219 FDA Orange Book

INSPECTIONS & REGISTRATIONS

2 FDA, 1 GDUFA

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1 GDUFA

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01 2Sciegen Pharmaceuticals Inc

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01 2No Action Indicated

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01 12013-09-18

02 12013-04-02

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01 2Hauppauge

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01

FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

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District Decision : No Action Indicated

Inspection End Date : 2013-04-02

ScieGen Pharmaceuticals

City : Hauppauge

State : NY

Country/Area : US

Zip : 11788-2005

District : NYK

Center : CDER

Project Area : Drug Quality Assurance

District Decision : No Action Indicated

Inspection End Date : 2013-04-02

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02

FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

FDA Audited

USA

euroPLX 86 Munich

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

District Decision : No Action Indicated

Inspection End Date : 2013-09-18

ScieGen Pharmaceuticals

City : Hauppauge

State : NY

Country/Area : US

Zip : 11788-2005

District : NYK

Center : CDER

Project Area : Drug Quality Assurance

District Decision : No Action Indicated

Inspection End Date : 2013-09-18

Product
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Stock Recap
#PipelineProspector

Data Compilation
#PharmaFlow

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