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Generated: December 16, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 071483

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NDA 071483 describes VERAPAMIL HYDROCHLORIDE, which is a drug marketed by Mylan, Abraxis Pharm, Bedford, Hospira, Intl Medication, Luitpold, Marsam Pharms Llc, Smith And Nephew, Solopak, Exela Pharma Scs Llc, Apotex Corp, Cadila Pharms Ltd, Glenmark Generics, Ivax Sub Teva Pharms, Par Pharm, Pliva, Sun Pharm Inds Inc, Actavis Elizabeth, Heritage Pharms Inc, Mutual Pharm, Sandoz, Sun Pharm Industries, Warner Chilcott, and Watson Labs, 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 071483

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

Medical Subject Heading (MeSH) Categories for 071483

Suppliers and Packaging for NDA: 071483

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
VERAPAMIL HYDROCHLORIDE verapamil hydrochloride TABLET;ORAL 071483 ANDA Mylan Pharmaceuticals Inc. 0378-0512 0378-0512-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0512-01)
VERAPAMIL HYDROCHLORIDE verapamil hydrochloride TABLET;ORAL 071483 ANDA Mylan Pharmaceuticals Inc. 0378-0772 0378-0772-05 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0772-05)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength120MG
Approval Date:Feb 15, 1989TE:ABRLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength80MG
Approval Date:Feb 15, 1989TE:ABRLD:No


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