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Serving hundreds of leading biopharmaceutical companies globally:

UBS
US Army
Covington
McKinsey
Federal Trade Commission
QuintilesIMS
Express Scripts
Baxter
Johnson and Johnson

Generated: April 24, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 080388

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NDA 080388 describes MEPERIDINE HYDROCHLORIDE, which is a drug marketed by Abbott, Baxter Hlthcare, Igi Labs Inc, Intl Medication, Parke Davis, Watson Labs, West-ward Pharms Int, Barr, Duramed Pharms Barr, Epic Pharma, Mikart, Specgx Llc, Sun Pharm Inds Inc, Sun Pharm Industries, Vintage Pharms, Wyeth Ayerst, Hospira, and Icu Medical Inc, and is included in forty-two NDAs. It is available from seven suppliers. Additional details are available on the MEPERIDINE HYDROCHLORIDE profile page.

The generic ingredient in MEPERIDINE HYDROCHLORIDE is meperidine hydrochloride. There are six drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the meperidine hydrochloride profile page.
Summary for 080388
Tradename:MEPERIDINE HYDROCHLORIDE
Applicant:Abbott
Ingredient:meperidine hydrochloride
Patents:0
Therapeutic Class:Analgesics
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 080388

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength25MG/ML
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Dow
Julphar
Johnson and Johnson
Boehringer Ingelheim
Harvard Business School
Mallinckrodt
McKinsey
Express Scripts
Farmers Insurance

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