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Approved Drug Products containing 78445 listed in the FDA Orange Book. Original Data : FDA Website

FDA Orange Book

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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Bora Pharmaceuticals- Making success more certain.

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Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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Axplora- The partner of choice for complex APIs.

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Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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01 2ENDO OPERATIONS

filter Dosage Reset all filters

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01 2TABLET, EXTENDED RELEASE;ORAL

filter Regulatory Info Reset all filters

2 All

01 2DISCN

filter Brand Name Reset all filters

2 All

01 2DIVALPROEX SODIUM

filter RLD Reset all filters

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01 2No

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Brand Name : DIVALPROEX SODIUM

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Brand Name : DIVALPROEX SODIUM

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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.

RLD : No

TE Code :

DIVALPROEX SODIUM

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : DIVALPROEX SODIUM

Dosage Strength : EQ 250MG VALPROIC ACID

Approval Date : 2009-02-26

Application Number : 78445

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Brand Name : DIVALPROEX SODIUM

Luxepack

Not Confirmed

Brand Name : DIVALPROEX SODIUM

Luxepack

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.

RLD : No

TE Code :

DIVALPROEX SODIUM

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : DIVALPROEX SODIUM

Dosage Strength : EQ 500MG VALPROIC ACID

Approval Date : 2009-08-04

Application Number : 78445

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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