Generated: August 24, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 073054
describes DOXEPIN HYDROCHLORIDE
, which is a drug marketed by Sun Pharm Inds, Par Pharm, Purepac Pharm, Teva Pharms, Wockhardt, Silarx, Pharm Assoc, Sandoz, Watson Labs, Quantum Pharmics, Mylan Pharms Inc, Actavis Elizabeth, Dava Pharms Inc, Amneal Pharms Co, New River, and Watson Labs Teva, and is included in fifty-six NDAs. It is available from twenty-four suppliers. Additional details are available on the DOXEPIN HYDROCHLORIDE profile page.
The generic ingredient in DOXEPIN HYDROCHLORIDE is doxepin hydrochloride. There are seven drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the doxepin hydrochloride profile page.
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Summary for product number 001
|Active Rx/OTC/Discontinued:||DISCN||Dosage:||CAPSULE;ORAL||Strength||EQ 10MG BASE|
|Approval Date:||Dec 28, 1990||TE:||RLD:||No|
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