Robert Schiff

FDA Filings

This page includes the latest FDA filings for Robert Schiff. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3003805036
FEI Number3003805036
NameRobert Schiff
Owner & OperatorPlastiape S.p.A
Contact Addressvia I Maggio, 8
Osnago IT-LC Lecco 23875 IT
US Agent
Importing Logistics Registration
ImporterNOVARTIS PHARMACEUTICAL CORPORATION
AddressONE HEALTH PLAZA
East Hanover, NJ 07936 UNITED STATES
Email Addresscorey.schmidt@novartis.com
Phone1 862 7782266
FAX1 973 7818891
Importer TypeRegistered NDA drug/device combinati
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1120 Bloomfield Avenue Suite 103
West Caldwell, NJ 07006 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Robert Schiff [Plastiape S.p.A]
Utibron? Neohaler?(indacaterol/glycopyrrolate) inhalation powder2016-03-14
Robert Schiff [Plastiape S.p.A]
Seebri ?Neohaler? (glycopyrrolate) Inhalation Powder Hard Capsules2016-03-14
Robert Schiff [Plastiape S.p.A]
Arcapta? Neohaler? (Indacaterol maleate inhalation powder) Hard Capsules2016-03-14

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