01 20ARIPIPRAZOLE
02 6BREXPIPRAZOLE
03 1CEDAZURIDINE; DECITABINE
04 2CILOSTAZOL
05 1DECITABINE
06 1FERRIC AMMONIUM CITRATE
07 3GREPAFLOXACIN HYDROCHLORIDE
08 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 32TABLET;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03 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 1100MG;35MG
05 210MG
06 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 415MG
08 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 11MG
10 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 220MG
12 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 32MG
14 430MG
15 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 13MG
17 145MG
18 14MG
19 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 25MG
22 1600MG/PACKET
23 160MG
24 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 1720MG/2.4ML (300MG/ML)
26 19.75MG/1.3ML (7.5MG/ML)
27 190MG
28 1960MG/3.2ML (300MG/ML)
29 1EQ 200MG BASE
30 1EQ 400MG BASE
31 1EQ 600MG BASE
01 14DISCN
02 28RX
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 : TABLET; ORAL
Proprietary Name : ABILIFY MYCITE KIT
Dosage Strength : 2MG
Approval Date : 2017-11-13
Application Number : 207202
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ABILIFY MYCITE KIT
Dosage Strength : 5MG
Approval Date : 2017-11-13
Application Number : 207202
RX/OTC/DISCN : RX
RLD : Yes
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 :
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