DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2DR REDDYS
02 2AJANTA PHARMA LTD
03 2ALKEM LABS LTD
04 2APOTEX
05 2BIONPHARMA
06 2ENDO OPERATIONS
07 2HETERO LABS LTD III
08 2INDOCO
09 2LUPIN LTD
10 2MANKIND PHARMA
11 2MEDLEY PHARMS
12 2MYLAN
13 1OYSTER POINT PHARMA
14 2PF PRISM CV
15 2PIRAMAL
16 2TEVA PHARMS USA
17 2WATSON LABS INC
18 2ZYDUS
01 1SPRAY;NASAL
02 2TABLET; ORAL
03 32TABLET;ORAL
01 2DISCN
02 29RX
03 4Blank
01 2CHANTIX
02 1TYRVAYA
03 2VARENICLINE
04 30VARENICLINE TARTRATE
01 28No
02 3Yes
03 4Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : VARENICLINE TARTRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE
Approval Date : 2024-10-01
Application Number : 215931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : VARENICLINE TARTRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Approval Date : 2024-10-01
Application Number : 215931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD :
TE Code :
Brand Name : VARENICLINE TARTRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE
Approval Date :
Application Number : 201808
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Brand Name : VARENICLINE TARTRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Approval Date :
Application Number : 201808
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code :
Brand Name : CHANTIX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2006-05-10
Application Number : 21928
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CHANTIX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2006-05-10
Application Number : 21928
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD :
TE Code :
Brand Name : VARENICLINE
Dosage Form : TABLET; ORAL
Dosage Strength : 0.5MG
Approval Date :
Application Number : 201920
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Brand Name : VARENICLINE
Dosage Form : TABLET; ORAL
Dosage Strength : 1MG
Approval Date :
Application Number : 201920
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code : AB
Brand Name : VARENICLINE TARTRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE
Approval Date : 2021-08-11
Application Number : 201785
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code : AB
Brand Name : VARENICLINE TARTRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Approval Date : 2021-08-11
Application Number : 201785
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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