01 1ALTRETAMINE
02 2AVATROMBOPAG MALEATE
03 7Anhydrous Perampanel
04 2Bexarotene
05 1DENILEUKIN DIFTITOX
06 6DONEPEZIL HYDROCHLORIDE
07 2ERIBULIN MESYLATE
08 2Eribulin
09 1Eribulinum Mesils
10 1FOSPROPOFOL DISODIUM
11 5LECANEMAB-IRMB
12 4LEMBOREXANT
13 8LENVATINIB (LENVATINIB MESYLATE)
14 2LENVATINIB MESYLATE
15 4Lenvatinib
16 6PERAMPANEL
17 16Perampanel
18 7RUFINAMIDE
19 3Rabeprazole Sodium
20 2Rabeprazole Sodium (Anhydrous)
21 7Rufinamide
22 4Rufinamidum
23 4Ziconotide
24 9Zonisamide
25 4lenvatinib
01 2AKARX INC
02 23EISAI INC
03 38EISAI LIMITED
04 2Eisai Ab
05 1Eisai Europe Limited
06 3Eisai Limited
07 23Eisai Ltd
08 18Eisai Pharma Ag
01 13Antic-calc Tablet, Film Coated
02 1Bexarotene 75Mg 100 Unita' Oral Use
03 8CAPSULE
04 3CAPSULE;ORAL
05 2Capsule
06 8Capsule, hard
07 1Capsule, soft
08 1Eribulina 0.88Mg 2Ml 1 Units Parenteral Use
09 11Film Coated Tablet
10 1GRANULE;ORAL
11 1Gastro-Resistant Tablet
12 2Hard Capsule
13 2INJECTABLE;INJECTION
14 2INJECTABLE;IV (INFUSION)
15 1INJECTABLE;SUBCUTANEOUS
16 2Infusion fluid, resolution
17 1Injectable Solution
18 1Injection fluid, resolution
19 1Lenvatinib 10Mg 30 Joined' Oral Use
20 1Lenvatinib 4Mg 30 Joined' Oral Use
21 2Oral Suspension
22 1Perampanel 10Mg 28 Combined Oral Use
23 1Perampanel 12Mg 28 Combined Oral Use
24 1Perampanel 2Mg 7 Units' Oral Use
25 1Perampanel 4Mg 28 Combined Oral Use
26 1Perampanel 6Mg 28 Combined Oral Use
27 1Perampanel 8Mg 28 Combined Oral Use
28 1Potion, suspension
29 1Rufinamide 100Mg 10 Units Oral Use
30 1Rufinamide 200Mg 60 Units Oral Use
31 1Rufinamide 400Mg 60 Units Oral Use
32 1SOLUTION
33 2SOLUTION;INTRAVENOUS
34 1SOLUTION;ORAL
35 1SUSPENSION;ORAL
36 11TABLET
37 2TABLET, ORALLY DISINTEGRATING;ORAL
38 9TABLET;ORAL
39 2Tablet
40 1VIAL
41 1Ziconotide 100Mcg 1Ml 1 Units Use Intrathecal
42 1Ziconotide 500Mcg 5Ml 1 Units Use Intrathecal
43 1Zonisamide 100Mg 56 Combined Oral Use
44 1Zonisamide 25Mg 14 Joined' Oral Use
45 1Zonisamide 50Mg 28 Combined Oral Use
01 10.44 mg/ml
02 10.5MG/ML
03 10.5mg/ml
04 11 Vial 1 ml 100 mcg/ml solution intrathecally
05 11 vial EV 0.88 mg 2 ml 0.44 mg/ml
06 11 vial of 5 ml 100 mcg/ml solution intrathecally
07 110 cpr riv 100 mg
08 310 mg
09 1100 cps 75 mg vial
10 2100 mcg/ml
11 4100 mg
12 1100MG
13 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 1100mg
15 11050MG/30ML (35MG/ML)
16 510MG
17 110MG/DOSE
18 510mg
19 212 mg
20 112MG
21 112MG/DOSE
22 112mg
23 114 cps 25 mg
24 114MG/DOSE
25 1150UG/ML
26 118MG/DOSE
27 11MG/2ML (0.5MG/ML)
28 11mg/2ml
29 12 mg
30 1200 mg
31 2200MG
32 1200MG/2ML
33 1200MG/2ML(100MG/ML)
34 1200mg
35 120MG
36 120MG/DOSE
37 220mg
38 123MG
39 124MG/DOSE
40 225 mg
41 128 cpr rev 4 mg
42 128 cpr riv 10 mg
43 128 cpr riv 12 mg
44 128 cpr riv 6 mg
45 128 cpr riv 8 mg
46 128 cps 50 mg
47 12MG
48 12mg
49 130 cps 10 mg
50 130 cps 4 mg
51 1360MG/1.8ML(200MG/ML)
52 34 mg
53 140 mg/ml
54 1400 mg
55 2400MG
56 1400mg
57 140MG/ML
58 140mg/ml
59 14MG
60 14MG/DOSE
61 34mg
62 150 mg
63 1500MG/5ML
64 1500MG/5ML(100MG/ML)
65 150MG
66 156 cps 100 mg
67 45MG
68 15MG/5ML
69 16 mg
70 160 cpr riv 200 mg
71 160 cpr riv div 400 mg
72 16MG
73 16mg
74 17 cpr riv 2 mg
75 175 mg
76 28 mg
77 18MG
78 18MG/DOSE
79 18mg
80 2EQ 10MG BASE
81 1EQ 20MG BASE
82 1EQ 4MG BASE
01 20Canada
02 18Italy
03 26Norway
04 1Spain
05 2Sweden
06 18Switzerland
07 25USA
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
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
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
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
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
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
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
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
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
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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