Generated: August 20, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 075090
, which is a drug marketed by Watson Labs, Amneal Pharms, Actavis Elizabeth, Apotex Inc, Mylan Pharms Inc, Zydus Pharms Usa Inc, Teva Pharms, Abbvie, Hi Tech Pharma, Mylan, Teva, Dava Pharms Inc, Fougera Pharms Inc, Chartwell Molecules, Hetero Labs Ltd V, Ivax Sub Teva Pharms, Actavis Mid Atlantic, Cadila Pharms Ltd, Lek Pharm, Taro, Roxane, Ranbaxy, Sun Pharm Inds Ltd, Carlsbad, Heritage Pharms Inc, Boscogen, Eurohlth Intl Sarl, Aurobindo Pharma Ltd, Fresenius Kabi Usa, Hospira, Mylan Labs Ltd, Teva Parenteral, Hikma Pharms Llc, Athenex Inc, and Apothecon, and is included in fifty-seven NDAs. It is available from fifty-eight suppliers. Additional details are available on the ACYCLOVIR profile page.
The generic ingredient in ACYCLOVIR is acyclovir sodium. There are fifty-five drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the acyclovir sodium profile page.
Summary for NDA: 075090
|Formulation / Manufacturing:||see details|
Pharmacology for NDA: 075090
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Summary for product number 001
|Approval Date:||Jan 26, 1999||TE:||AB||RLD:||No|
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