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01 1ALTRETAMINE
02 2AVATROMBOPAG MALEATE
03 1DENILEUKIN DIFTITOX
04 6DONEPEZIL HYDROCHLORIDE
05 1ERIBULIN MESYLATE
06 1FOSPROPOFOL DISODIUM
07 4LECANEMAB-IRMB
08 2LEMBOREXANT
09 2LENVATINIB MESYLATE
10 4RUFINAMIDE
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01 3CAPSULE;ORAL
02 1GRANULE;ORAL
03 4INJECTABLE;INJECTION
04 2SOLUTION;INTRAVENOUS
05 1SOLUTION;ORAL
06 1SUSPENSION;ORAL
07 2TABLET, ORALLY DISINTEGRATING;ORAL
08 9TABLET;ORAL
09 1VIAL
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01 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 11050MG/30ML (35MG/ML)
03 310MG
04 1150UG/ML
05 11MG/2ML (0.5MG/ML)
06 1200MG
07 1200MG/2ML
08 1200MG/2ML(100MG/ML)
09 123MG
10 1400MG
11 140MG/ML
12 1500MG/5ML
13 1500MG/5ML(100MG/ML)
14 150MG
15 35MG
16 15MG/5ML
17 2EQ 10MG BASE
18 1EQ 20MG BASE
19 1EQ 4MG BASE
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01 6DISCN
02 13RX
03 5Blank
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RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : HEXALEN
Dosage Strength : 50MG
Approval Date : 1990-12-26
Application Number : 19926
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DOPTELET
Dosage Strength : EQ 20MG BASE
Approval Date : 2018-05-21
Application Number : 210238
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : GRANULE; ORAL
Proprietary Name : DOPTELET SPRINKLE
Dosage Strength : EQ 10MG BASE
Approval Date : 2025-07-24
Application Number : 219696
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD :
TE Code :
Dosage Form : VIAL
Proprietary Name : ONTAK
Dosage Strength : 150UG/ML
Approval Date :
Application Number : 103767
RX/OTC/DISCN :
RLD :
TE Code :

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RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARICEPT
Dosage Strength : 10MG
Approval Date : 1996-11-25
Application Number : 20690
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARICEPT
Dosage Strength : 5MG
Approval Date : 1996-11-25
Application Number : 20690
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : ARICEPT
Dosage Strength : 5MG/5ML
Approval Date : 2004-10-18
Application Number : 21719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : ARICEPT ODT
Dosage Strength : 5MG
Approval Date : 2004-10-18
Application Number : 21720
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : ARICEPT ODT
Dosage Strength : 10MG
Approval Date : 2004-10-18
Application Number : 21720
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARICEPT
Dosage Strength : 23MG
Approval Date : 2010-07-23
Application Number : 22568
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

Eisai Inc is a supplier offers 3 products (APIs, Excipients or Intermediates).
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