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McKesson
Chubb
Medtronic
Federal Trade Commission
Deloitte
Teva
Cipla
Farmers Insurance
UBS

Generated: June 18, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070752

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NDA 070752 describes NALBUPHINE, which is a drug marketed by Abraxis Pharm, Abbott, Abbvie, Barr, Hospira, and Igi Labs Inc, and is included in fifteen NDAs. Additional details are available on the NALBUPHINE profile page.

The generic ingredient in NALBUPHINE is nalbuphine hydrochloride. There are six drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the nalbuphine hydrochloride profile page.
Summary for 070752
Tradename:NALBUPHINE
Applicant:Abraxis Pharm
Ingredient:nalbuphine hydrochloride
Patents:0
Therapeutic Class:Analgesics
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 070752

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength20MG/ML
Approval Date:Sep 24, 1986TE:RLD:No

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Harvard Business School
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