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01 1ALTRETAMINE
02 2AVATROMBOPAG MALEATE
03 7Anhydrous Perampanel
04 1Bexarotene
05 1DENILEUKIN DIFTITOX
06 6DONEPEZIL HYDROCHLORIDE
07 2ERIBULIN MESYLATE
08 1Eribulin
09 1Eribulinum Mesils
10 1FOSPROPOFOL DISODIUM
11 1LECANEMAB
12 3LECANEMAB-IRMB
13 4LEMBOREXANT
14 8LENVATINIB (LENVATINIB MESYLATE)
15 2LENVATINIB MESYLATE
16 4Lenvatinib
17 6PERAMPANEL
18 6Perampanel
19 7RUFINAMIDE
20 5Rabeprazole Sodium
21 2Rabeprazole Sodium (Anhydrous)
22 3Rufinamide
23 4Rufinamidum
24 2Ziconotide
25 3Zonisamide
26 2lenvatinib
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01 2AKARX INC
02 21EISAI INC
03 39EISAI LIMITED
04 4Eisai Ab
05 1Eisai Ltd
06 18Eisai Pharma Ag
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01 1Bexarotene 75Mg 100 Unita' Oral Use
02 8CAPSULE
03 3CAPSULE;ORAL
04 2Capsule
05 2Enteric-Coated Tablet
06 1Eribulina 0.88Mg 2Ml 1 Units Parenteral Use
07 11Film Coated Tablet
08 1GRANULE;ORAL
09 1Gastro-Resistant Tablet
10 2Hard Capsule
11 2INJECTABLE;INJECTION
12 1INJECTABLE;SUBCUTANEOUS
13 1Injectable Solution
14 1Lenvatinib 10Mg 30 Joined' Oral Use
15 1Lenvatinib 4Mg 30 Joined' Oral Use
16 2Oral Suspension
17 1Perampanel 10Mg 28 Combined Oral Use
18 1Perampanel 12Mg 28 Combined Oral Use
19 1Perampanel 2Mg 7 Units' Oral Use
20 1Perampanel 4Mg 28 Combined Oral Use
21 1Perampanel 6Mg 28 Combined Oral Use
22 1Perampanel 8Mg 28 Combined Oral Use
23 1Rufinamide 100Mg 10 Units Oral Use
24 1Rufinamide 200Mg 60 Units Oral Use
25 1Rufinamide 400Mg 60 Units Oral Use
26 2SOLUTION
27 2SOLUTION;INTRAVENOUS
28 1SOLUTION;ORAL
29 1SUSPENSION;ORAL
30 11TABLET
31 2TABLET, ORALLY DISINTEGRATING;ORAL
32 9TABLET;ORAL
33 2Tablet
34 1VIAL
35 1Ziconotide 100Mcg 1Ml 1 Units Use Intrathecal
36 1Ziconotide 500Mcg 5Ml 1 Units Use Intrathecal
37 1Zonisamide 100Mg 56 Combined Oral Use
38 1Zonisamide 25Mg 14 Joined' Oral Use
39 1Zonisamide 50Mg 28 Combined Oral Use
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01 10.5MG/ML
02 10.5mg/ml
03 11 Vial 1 ml 100 mcg/ml solution intrathecally
04 11 vial EV 0.88 mg 2 ml 0.44 mg/ml
05 11 vial of 5 ml 100 mcg/ml solution intrathecally
06 110 cpr riv 100 mg
07 1100 cps 75 mg vial
08 1100MG
09 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1100MG/ML
11 1100mg
12 11050MG/30ML (35MG/ML)
13 510MG
14 110MG/DOSE
15 610mg
16 112MG
17 112MG/DOSE
18 112mg
19 114 cps 25 mg
20 114MG/DOSE
21 1150UG/ML
22 118MG/DOSE
23 11MG/2ML (0.5MG/ML)
24 11mg/2ml
25 2200MG
26 1200MG/2ML
27 1200mg
28 120MG
29 120MG/DOSE
30 320mg
31 123MG
32 124MG/DOSE
33 128 cpr rev 4 mg
34 128 cpr riv 10 mg
35 128 cpr riv 12 mg
36 128 cpr riv 6 mg
37 128 cpr riv 8 mg
38 128 cps 50 mg
39 12MG
40 12mg
41 130 cps 10 mg
42 130 cps 4 mg
43 1360MG/1.8ML(200MG/ML)
44 2400MG
45 1400mg
46 140MG/ML
47 140mg/ml
48 14MG
49 14MG/DOSE
50 34mg
51 1500MG/5ML
52 150MG
53 156 cps 100 mg
54 45MG
55 15MG/5ML
56 160 cpr riv 200 mg
57 160 cpr riv div 400 mg
58 16MG
59 16mg
60 17 cpr riv 2 mg
61 18MG
62 18MG/DOSE
63 18mg
64 2EQ 10MG BASE
65 1EQ 20MG BASE
66 1EQ 4MG BASE
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01 21Canada
02 2Denmark
03 18Italy
04 1Spain
05 2Sweden
06 18Switzerland
07 23USA
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : HEXALEN
Dosage Strength : 50MG
Packaging :
Approval Date : 1990-12-26
Application Number : 19926
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Fycompa
Dosage Strength : 2mg
Packaging :
Approval Date : 14/12/2012
Application Number : 62440
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Fycompa
Dosage Strength : 4mg
Packaging :
Approval Date : 14/12/2012
Application Number : 62440
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Fycompa
Dosage Strength : 6mg
Packaging :
Approval Date : 14/12/2012
Application Number : 62440
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Fycompa
Dosage Strength : 8mg
Packaging :
Approval Date : 14/12/2012
Application Number : 62440
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Fycompa
Dosage Strength : 10mg
Packaging :
Approval Date : 14/12/2012
Application Number : 62440
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Fycompa
Dosage Strength : 12mg
Packaging :
Approval Date : 14/12/2012
Application Number : 62440
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Oral Suspension
Brand Name : Fycompa
Dosage Strength : 0.5mg/ml
Packaging :
Approval Date : 16/04/2020
Application Number : 67665
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : DOPTELET
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2018-05-21
Application Number : 210238
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : GRANULE;ORAL
Brand Name : DOPTELET SPRINKLE
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2025-07-24
Application Number : 219696
Regulatory Info : RX
Registration Country : USA

Eisai Inc is a supplier offers 3 products (APIs, Excipients or Intermediates).
Find a price of MOH040 bulk with DMF offered by Eisai Inc
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