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Generated: February 25, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 040874

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NDA 040874 describes DIPYRIDAMOLE, which is a drug marketed by Athenex Inc, Fresenius Kabi Usa, Hospira, Mylan Labs Ltd, Teva Pharms Usa, West-ward Pharms Int, Barr, Glenmark Generics, Idt Australia Ltd, Impax Labs, Lannett, Murty Pharms, Oxford Pharms, Purepac Pharm, Watson Labs, and Zydus Pharms Usa Inc, and is included in twenty-two NDAs. It is available from ten suppliers. Additional details are available on the DIPYRIDAMOLE profile page.

The generic ingredient in DIPYRIDAMOLE is dipyridamole. There are eighteen drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the dipyridamole profile page.
Summary for 040874
Tradename:DIPYRIDAMOLE
Applicant:Zydus Pharms Usa Inc
Ingredient:dipyridamole
Patents:0
Therapeutic Class:Blood Products/Modifiers/ Volume Expanders
Formulation / Manufacturing:see details
Pharmacology for NDA: 040874
Physiological EffectDecreased Platelet Aggregation
Medical Subject Heading (MeSH) Categories for 040874
Suppliers and Packaging for NDA: 040874
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DIPYRIDAMOLE dipyridamole TABLET;ORAL 040874 ANDA Cadila Healthcare Limited 65841-662 N 65841-662-01
DIPYRIDAMOLE dipyridamole TABLET;ORAL 040874 ANDA Cadila Healthcare Limited 65841-662 N 65841-662-30

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength25MG
Approval Date:Jan 28, 2008TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength50MG
Approval Date:Jan 28, 2008TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength75MG
Approval Date:Jan 28, 2008TE:ABRLD:No

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