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Last Updated: December 15, 2024

Details for New Drug Application (NDA): 207611


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NDA 207611 describes VALPROIC ACID, which is a drug marketed by Bionpharma, Catalent, Hibrow Hlthcare, Par Pharm, Scherer Rp, Sun Pharm Inds Ltd, Upsher Smith Labs, Ani Pharms, Chartwell Rx, Hikma, Lannett Co Inc, Nostrum Labs Inc, Pharm Assoc, Pharmobedient Cnsltg, and Quagen, and is included in fifteen NDAs. It is available from seventeen suppliers. Additional details are available on the VALPROIC ACID profile page.

The generic ingredient in VALPROIC ACID is valproic acid. There are seventeen drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the valproic acid profile page.
Summary for 207611
Tradename:VALPROIC ACID
Applicant:Hibrow Hlthcare
Ingredient:valproic acid
Patents:0
Pharmacology for NDA: 207611
Medical Subject Heading (MeSH) Categories for 207611
Suppliers and Packaging for NDA: 207611
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
VALPROIC ACID valproic acid CAPSULE;ORAL 207611 ANDA McKesson Corporation dba SKY Packaging 63739-253 63739-253-40 100 CAPSULE in 1 BOTTLE (63739-253-40)
VALPROIC ACID valproic acid CAPSULE;ORAL 207611 ANDA Direct_Rx 72189-267 72189-267-30 30 CAPSULE in 1 BOTTLE (72189-267-30)

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength250MG
Approval Date:Aug 5, 2019TE:RLD:No

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