01 2ABACAVIR SULFATE
02 2ABACAVIR SULFATE; DOLUTEGRAVIR SODIUM; LAMIVUDINE
03 1ABACAVIR SULFATE; LAMIVUDINE
04 1ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE
05 1CABOTEGRAVIR
06 1CABOTEGRAVIR SODIUM
07 2CABOTEGRAVIR; RILPIVIRINE
08 2DELAVIRDINE MESYLATE
09 4DOLUTEGRAVIR SODIUM
10 1DOLUTEGRAVIR SODIUM; LAMIVUDINE
11 1DOLUTEGRAVIR SODIUM; RILPIVIRINE HYDROCHLORIDE
12 2FOSAMPRENAVIR CALCIUM
13 1FOSTEMSAVIR TROMETHAMINE
14 3LAMIVUDINE
15 1LAMIVUDINE; ZIDOVUDINE
16 5MARAVIROC
17 5ZIDOVUDINE
01 1CAPSULE;ORAL
02 1INJECTABLE;INJECTION
03 4SOLUTION;ORAL
04 3SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
05 1SUSPENSION;ORAL
06 1TABLET, EXTENDED RELEASE;ORAL
07 2TABLET, FOR SUSPENSION;ORAL
08 22TABLET;ORAL
01 2100MG
02 210MG/ML
03 2150MG
04 1150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 2200MG
06 120MG/ML
07 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 2300MG
09 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1400MG/2ML (200MG/ML);600MG/2ML (300MG/ML)
11 150MG/5ML
12 1600MG/3ML (200MG/ML)
13 1600MG/3ML (200MG/ML);900MG/3ML (300MG/ML)
14 175MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 1EQ 20MG BASE/ML
17 1EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1EQ 300MG BASE;150MG;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 1EQ 30MG BASE
21 1EQ 50MG BASE
22 1EQ 50MG BASE/ML
23 1EQ 50MG BASE;300MG
24 1EQ 50MG BASE;EQ 25MG BASE
25 1EQ 5MG BASE
26 1EQ 600MG BASE
27 1EQ 600MG BASE;300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 1EQ 600MG BASE;EQ 50MG BASE;300MG
29 1EQ 60MG BASE;EQ 5MG BASE;30MG
30 1EQ 700MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 14DISCN
02 21RX
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ZIAGEN
Dosage Strength : EQ 300MG BASE **Federal ...
Approval Date : 1998-12-17
Application Number : 20977
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AA
Dosage Form : SOLUTION; ORAL
Proprietary Name : ZIAGEN
Dosage Strength : EQ 20MG BASE/ML
Approval Date : 1998-12-17
Application Number : 20978
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AA
RLD : Yes
TE Code :
ABACAVIR SULFATE; DOLUTEGRAVIR SODIUM; LAMIVUDINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIUMEQ
Dosage Strength : EQ 600MG BASE;EQ 50MG BA...
Approval Date : 2014-08-22
Application Number : 205551
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ABACAVIR SULFATE; DOLUTEGRAVIR SODIUM; LAMIVUDINE
Dosage Form : TABLET, FOR SUSPENSION; ORAL
Proprietary Name : TRIUMEQ PD
Dosage Strength : EQ 60MG BASE;EQ 5MG BASE...
Approval Date : 2022-03-30
Application Number : 215413
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : EPZICOM
Dosage Strength : EQ 600MG BASE;300MG **Fe...
Approval Date : 2004-08-02
Application Number : 21652
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIZIVIR
Dosage Strength : EQ 300MG BASE;150MG;300M...
Approval Date : 2000-11-14
Application Number : 21205
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SUSPENSION, EXTENDED RELEASE; ...
Proprietary Name : APRETUDE
Dosage Strength : 600MG/3ML (200MG/ML)
Approval Date : 2021-12-20
Application Number : 215499
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : VOCABRIA
Dosage Strength : EQ 30MG BASE
Approval Date : 2021-01-21
Application Number : 212887
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SUSPENSION, EXTENDED RELEASE; ...
Proprietary Name : CABENUVA KIT
Dosage Strength : 400MG/2ML (200MG/ML);600...
Approval Date : 2021-01-21
Application Number : 212888
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SUSPENSION, EXTENDED RELEASE; ...
Proprietary Name : CABENUVA KIT
Dosage Strength : 600MG/3ML (200MG/ML);900...
Approval Date : 2021-01-21
Application Number : 212888
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
