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Generated: September 19, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 073568

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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.

Summary for NDA: 073568

Tradename:
1
Applicant:
1
Ingredient:
1
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Suppliers and Packaging for NDA: 073568

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
VERAPAMIL HYDROCHLORIDE
verapamil hydrochloride
TABLET, EXTENDED RELEASE;ORAL 073568 ANDA NCS HealthCare of KY, Inc dba Vangard Labs 0615-3589 0615-3589-31 31 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-3589-31)
VERAPAMIL HYDROCHLORIDE
verapamil hydrochloride
TABLET, EXTENDED RELEASE;ORAL 073568 ANDA NCS HealthCare of KY, Inc dba Vangard Labs 0615-3589 0615-3589-39 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-3589-39)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength240MG
Approval Date:Jul 31, 1992TE:ABRLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength120MG
Approval Date:Oct 10, 1997TE:ABRLD:No


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QuintilesIMS
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