DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 080822
describes DIPHENHYDRAMINE HYDROCHLORIDE
, which is a drug marketed by Whiteworth Town Plsn, Elkins Sinn, Pioneer Pharms, Mutual Pharm, Impax Labs, Cumberland Swan, Pharm Assoc, Halsey, Hi Tech Pharma, West-ward Pharms Int, Alra, Kv Pharm, Bel Mar, Heather, Pvt Form, Watson Labs, Vangard, Sandoz, Nexgen Pharma Inc, Roxane, Lederle, Purepac Pharm, Barr, Lannett, Superpharm, Hospira, Cenci, Newtron Pharms, Perrigo, Ivax Sub Teva Pharms, App Pharms, Lyphomed, Hikma Intl Pharms, Watson Labs Teva, Teva, Bundy, Anabolic, LNK, Wyeth Ayerst, Naska, Eurohlth Intl Sarl, Mk Labs, Sun Pharm Inds, Valeant Pharm Intl, Alpharma Us Pharms, Mylan Institutional, Fresenius Kabi Usa, Abraxis Pharm, and Intl Medication, and is included in seventy-three NDAs. It is available from sixteen suppliers. Additional details are available on the DIPHENHYDRAMINE HYDROCHLORIDE profile page.
The generic ingredient in DIPHENHYDRAMINE HYDROCHLORIDE is diphenhydramine hydrochloride. There are twenty-three drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the diphenhydramine hydrochloride profile page.
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Summary for product number 001
|Approval Date:||Approved Prior to Jan 1, 1982||TE:||RLD:||No|
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