BILLS-117hr2891ih.pdf
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DATE (19)
2003
30 days
year 2019
the preceding calendar year
6
2003
12-year
12-month
December 31
1ST SESSION H. R. 2891
APRIL 28, 2021
15 U.S.C. 12(a
year 2020
180-DAY
later than 6 years
3-year
1112
21
PERIOD
1 year
42 U.S.C.
EVENT (1)
the ‘‘Preserve Access
FAC (6)
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GPE (5)
the United States
the District of Columbia Circuit
United States
New York
the United States of America
LOC (2)
IH
Approved
NORP (1)
sist
ORG (42)
DSK79L0C42PROD
ANDA
NDA
U.S.C.
Commission
SEC
the Federal Trade
uct
the Federal Food, Drug
the Public Health Service Act
Federal Food, Drug
Federal Trade Commission
the Food and Drug Administration
Senate
NDA.—The
GENERAL.—If
the United States Court
Medicare
the Federal Food
14
Commission
the Department of Justice
the House of Representatives
United States Patent and Trademark Office
the Federal Trade Commission
Legal Services
the Public Health Service
Congress
Prescription Drug, Improvement
Department of Labor
Federal
House of Representa-
the Committee on
Energy and Commerce
FDA
360cc
Drug, Improvement
the Federal Trade Commis-
the Committee on the Judiciary
the Committee on the Judiciary of
the Bureau of Labor Statistics
PERSON (5)
BUCK
NADLER
CAROLYN B.
CICILLINE
Act
Topic Classifications
congressional legislation
95.3%
public health
60.2%
government oversight
43.6%
Extracted Keywords
biosimilar biological
biosimilar
biological product
patent
biological
product
generic
prescription drug
drug
prescription
delay
proceeding
entry
claim
biological products
Forensic Analysis
PDF Metadata
- Creator
- U.S. Gov. Printing Office -- G.S.D.D.
- ModDate
- D:20221230141039Z
- Producer
- Acrobat Distiller 21.0 (Windows); modified using iText® Core 7.2.3 (production version) ©2000-2022 iText Group NV, Government Publishing Office
- CreationDate
- D:20210617062453-04'00'
Sentiment
Polarity
Neutral
0.072
Subjectivity
43%
Objective