01 20ARIPIPRAZOLE
02 6BREXPIPRAZOLE
03 2CILOSTAZOL
04 1DECITABINE
05 1FERRIC AMMONIUM CITRATE
06 3GREPAFLOXACIN HYDROCHLORIDE
07 8TOLVAPTAN
01 1FOR SOLUTION;ORAL
02 1INJECTABLE;INTRAMUSCULAR
03 1INJECTABLE;INTRAVENOUS
04 1SOLUTION;ORAL
05 2SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
06 4TABLET, ORALLY DISINTEGRATING;ORAL
07 31TABLET;ORAL
01 10.25MG
02 10.5MG
03 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 210MG
05 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 415MG
07 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 11MG
09 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 220MG
11 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 32MG
13 430MG
14 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 13MG
16 145MG
17 14MG
18 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 25MG
21 1600MG/PACKET
22 160MG
23 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 1720MG/2.4ML (300MG/ML)
25 19.75MG/1.3ML (7.5MG/ML)
26 190MG
27 1960MG/3.2ML (300MG/ML)
28 1EQ 200MG BASE
29 1EQ 400MG BASE
30 1EQ 600MG BASE
01 20DISCN
02 21RX
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 10MG
Approval Date : 2002-11-15
Application Number : 21436
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 15MG
Approval Date : 2002-11-15
Application Number : 21436
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 20MG
Approval Date : 2002-11-15
Application Number : 21436
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 30MG
Approval Date : 2002-11-15
Application Number : 21436
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 5MG
Approval Date : 2002-11-15
Application Number : 21436
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 2MG
Approval Date : 2002-11-15
Application Number : 21436
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : ABILIFY
Dosage Strength : 1MG/ML **Federal Registe...
Approval Date : 2004-12-10
Application Number : 21713
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INTRAMUSCULAR
Proprietary Name : ABILIFY
Dosage Strength : 9.75MG/1.3ML (7.5MG/ML)
Approval Date : 2006-09-20
Application Number : 21866
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : SUSPENSION, EXTENDED RELEASE; ...
Proprietary Name : ABILIFY ASIMTUFII
Dosage Strength : 720MG/2.4ML (300MG/ML)
Approval Date : 2023-04-27
Application Number : 217006
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SUSPENSION, EXTENDED RELEASE; ...
Proprietary Name : ABILIFY ASIMTUFII
Dosage Strength : 960MG/3.2ML (300MG/ML)
Approval Date : 2023-04-27
Application Number : 217006
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
Otsuka Chemical Co Ltd is a supplier offers 13 products (APIs, Excipients or Intermediates).
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