Generated: September 19, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 073568
describes VERAPAMIL HYDROCHLORIDE
, which is a drug marketed by Glenmark Generics, Mylan, Luitpold, Actavis Elizabeth, Pliva, Sandoz, Watson Labs, Exela Pharma Scs Llc, Sun Pharm Inds Inc, Ivax Sub Teva Pharms, Marsam Pharms Llc, Hospira, Warner Chilcott, Abraxis Pharm, Intl Medication, Par Pharm, Cadila Pharms Ltd, Apotex Corp, Heritage Pharms Inc, Mutual Pharm, Bedford, Sun Pharm Inds, Solopak, and Smith And Nephew, and is included in fifty-four NDAs. It is available from thirty-seven suppliers. Additional details are available on the VERAPAMIL HYDROCHLORIDE profile page.
The generic ingredient in VERAPAMIL HYDROCHLORIDE is verapamil hydrochloride. There are sixteen drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the verapamil hydrochloride profile page.
Pharmacology for NDA: 073568
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Summary for product number 001
|Active Rx/OTC/Discontinued:||RX||Dosage:||TABLET, EXTENDED RELEASE;ORAL||Strength||240MG|
|Approval Date:||Jul 31, 1992||TE:||AB||RLD:||No|
Summary for product number 002
|Active Rx/OTC/Discontinued:||RX||Dosage:||TABLET, EXTENDED RELEASE;ORAL||Strength||120MG|
|Approval Date:||Oct 10, 1997||TE:||AB||RLD:||No|
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