Generated: December 18, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 204312
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, which is a drug marketed by Aurobindo Pharma Ltd, Fresenius Kabi Usa, Hikma Farmaceutica, Hospira Inc, Jubilant Generics, Luitpold, Mylan Labs Ltd, Sagent Pharms, Sun Pharm Inds Ltd, X Gen Pharms, Actavis Mid Atlantic, Allied Pharma Inc, Amneal Pharms, Apotex Inc, Breckenridge Pharm, Hetero Labs Ltd Iii, Hi-tech Pharmacal, Lupin Ltd, Orit Labs Llc, Pharm Assoc, Silarx, Taro, Tolmar, Tris Pharma Inc, Vintage Pharms, Wockhardt, Actavis Elizabeth, Actavis Labs Fl Inc, Anchen Pharms, Dexcel Pharma, Eci Pharms Llc, Intellipharmaceutics, Lotus Pharm Co Ltd, Mylan Pharms Inc, Pharmadax Inc, Pharmtak Inc, Prinston Inc, Rouses Point Pharms, Sandoz, Sun Pharm Industries, Sun Pharma Global, Teva Pharms, Torrent Pharms Ltd, Virtus Pharms, Accord Hlthcare, Aci Healthcare Ltd, Acic Pharms, Ajanta Pharma, Aurobindo Pharma, Dr Reddys Labs Ltd, Invagen Pharms, Lupin, Mylan, Orchid Hlthcare, Secan Pharms, Torrent Pharms, Watson Labs Inc, Zydus Pharms Usa Inc, Gland Pharma Ltd, and Hq Speciality Pharma, and is included in eighty-three NDAs. It is available from ninety-four suppliers. Additional details are available on the LEVETIRACETAM profile page.
The generic ingredient in LEVETIRACETAM is levetiracetam. There are thirty-five drug master file entries for this compound. One hundred suppliers are listed for this compound. Additional details are available on the levetiracetam profile page.
Pharmacology for NDA: 204312
Suppliers and Packaging for NDA: 204312
||National Drug Code
||AuroMedics Pharma LLC
||10 VIAL, SINGLE-USE in 1 CARTON (55150-177-05) > 5 mL in 1 VIAL, SINGLE-USE
|Complete Access Available with Subscription
Summary for product number 001
|Active Rx/OTC/Discontinued:||RX||Dosage:||INJECTABLE;IV (INFUSION)||Strength||500MG/5ML (100MG/ML)|
|Approval Date:||Feb 1, 2016||TE:||AP||RLD:||No|
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