01 10ABBVIE
02 1ABBOTT
03 1AMNEAL
04 3AUROBINDO PHARMA LTD
05 2CIPLA
06 4CIPLA LIMITED
07 1CIPLA LTD
08 1EMCURE PHARMS LTD
09 3HETERO LABS LTD III
10 1HIKMA
11 1LANNETT CO INC
12 2LAURUS
13 2MACLEODS PHARMS LTD
14 1MATRIX LABS LTD
15 3MYLAN LABS LTD
16 2MYLAN PHARMA
17 2MYLAN PHARMS INC
18 1NORVIUM BIOSCIENCE
01 5CAPSULE;ORAL
02 1PELLETS;ORAL
03 1POWDER;ORAL
04 1SOLUTION; ORAL
05 3SOLUTION;ORAL
06 1TABLET, EXTENDED RELEASE;ORAL
07 10TABLET; ORAL
08 19TABLET;ORAL
01 7DISCN
02 20RX
03 14Blank
01 1ATAZANAVIR SULFATE AND RITONAVIR
02 1ATAZANAVIR SULFATE; RITONAVIR
03 1ATAZANAVIR SULFATE;RITONAVIR;LAMIVUDINE;ZIDOVUDINE
04 1DARUNAVIR AND RITONAVIR
05 4KALETRA
06 10LOPINAVIR AND RITONAVIR
07 6LOPINAVIR; RITONAVIR
08 5NORVIR
09 10RITONAVIR
10 1TECHNIVIE
11 1VIEKIRA XR
01 18No
02 9Yes
03 14Blank
RLD : Yes
TE Code :
Brand Name : NORVIR
Dosage Form : SOLUTION;ORAL
Dosage Strength : 80MG/ML
Approval Date : 1996-03-01
Application Number : 20659
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NORVIR
Dosage Form : CAPSULE;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1999-06-29
Application Number : 20945
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : KALETRA
Dosage Form : CAPSULE;ORAL
Dosage Strength : 133.3MG;33.3MG
Approval Date : 2000-09-15
Application Number : 21226
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AA
Brand Name : KALETRA
Dosage Form : SOLUTION;ORAL
Dosage Strength : 80MG/ML;20MG/ML
Approval Date : 2000-09-15
Application Number : 21251
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AA
RLD : Yes
TE Code : AB
Brand Name : KALETRA
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG;50MG
Approval Date : 2005-10-28
Application Number : 21906
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : KALETRA
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG;25MG
Approval Date : 2007-11-09
Application Number : 21906
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : NORVIR
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Approval Date : 2010-02-10
Application Number : 22417
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
OMBITASVIR; PARITAPREVIR; RITONAVIR
Brand Name : TECHNIVIE
Dosage Form : TABLET;ORAL
Dosage Strength : 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2015-07-24
Application Number : 207931
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR
Brand Name : VIEKIRA XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2016-07-22
Application Number : 208624
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NORVIR
Dosage Form : POWDER;ORAL
Dosage Strength : 100MG/PACKET
Approval Date : 2017-06-07
Application Number : 209512
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
