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Last Updated: November 24, 2024

Details for New Drug Application (NDA): 040362


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NDA 040362 describes PREDNISONE, which is a drug marketed by Hikma, Xttrium Labs Inc, Actavis Labs Fl Inc, Allied, Am Therap, Amneal, Amneal Pharms Ny, Aurobindo Pharma Ltd, Bundy, Chartwell Molecular, Chartwell Rx, Contract Pharmacal, Duramed Pharms Barr, Elkins Sinn, Endo Operations, Everylife, Ferrante, Geneyork Pharms, Halsey, Heather, Hikma Pharms, Impax Labs, Inwood Labs, Ivax Sub Teva Pharms, Jubilant Cadista, Kv Pharm, Lederle, Marshall Pharma, Mutual Pharm, Mylan, Novitium Pharma, Nylos, Panray, Pharmavite, Phoenix Labs Ny, Purepac Pharm, Pvt Form, Rexall, Rising, Roxane, Sandoz, Scherer Labs, Sperti, Strides Pharma, Sun Pharm Industries, Superpharm, Teva, UDL, Upsher Smith, Valeant Pharm Intl, Vangard, Vitarine, Watson Labs, and Whiteworth Town Plsn, and is included in one hundred and sixteen NDAs. It is available from fifty suppliers. Additional details are available on the PREDNISONE profile page.

The generic ingredient in PREDNISONE is prednisone. There are sixteen drug master file entries for this compound. Fifty-one suppliers are listed for this compound. Additional details are available on the prednisone profile page.
Summary for 040362
Tradename:PREDNISONE
Applicant:Jubilant Cadista
Ingredient:prednisone
Patents:0
Pharmacology for NDA: 040362
Medical Subject Heading (MeSH) Categories for 040362
Suppliers and Packaging for NDA: 040362
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PREDNISONE prednisone TABLET;ORAL 040362 ANDA Major Pharmaceuticals 0904-7127 0904-7127-61 100 BLISTER PACK in 1 CARTON (0904-7127-61) / 1 TABLET in 1 BLISTER PACK
PREDNISONE prednisone TABLET;ORAL 040362 ANDA AvKARE 42291-727 42291-727-10 1000 TABLET in 1 BOTTLE (42291-727-10)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength10MG
Approval Date:Aug 29, 2001TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength5MG
Approval Date:Aug 29, 2001TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength20MG
Approval Date:Jun 29, 2005TE:ABRLD:No

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