Viewing data from:

TYZEKA

NDA

TELBIVUDINE | N022011 | NOVARTIS PHARMACEUTICALS CORP

1 strength0 unique patents0 unique exclusivities

PTAB Proceedings

No IPR/PGR/CBM challenges found at the Patent Trial and Appeal Board

Patent Reexaminations

No ex parte or inter partes reexamination proceedings found at USPTO

Hatch-Waxman Litigation

No ANDA patent litigation cases (NOS 835) matched from PACER

Citizen Petitions

No FDA citizen petitions matched from Regulations.gov

Clinical Trials

No clinical trials found on ClinicalTrials.gov for this drug

API Supply Chain0 active DMFs2 inactive

0 active API suppliers hold Drug Master Files for this ingredient. Limited supplier base — potential supply chain risk.

RANBAXY LABORATORIES LTDInactiveTELBIVUDINE

DMF 244292010

SICHUAN XIELI PHARMACEUTICAL CO LTDInactiveTELBIVUDINE

DMF 264932012

Source: FDA Drug Master Files (fda.gov). Type II API DMFs matched by ingredient.

Approval Letters

11 letters from Drugs@FDA

Source: Drugs@FDA application documents.

Products (1)

#001 — 600MG

RLD

0 patents0 exclusivities▴

TABLET;ORAL | Approved: Oct 25, 2006

No patent or exclusivity listings for this strength.