DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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01 2DR REDDYS
02 2AJANTA PHARMA LTD
03 2ALKEM LABS LTD
04 2APOTEX
05 2ENDO OPERATIONS
06 2HETERO LABS LTD III
07 2INDOCO
08 2LUPIN LTD
09 2MACLEODS PHARMS LTD
10 2MANKIND PHARMA
11 2MEDLEY PHARMS
12 2MYLAN
13 2NE RX PHARMA
14 1OYSTER POINT PHARMA
15 2PF PRISM CV
16 2PIRAMAL
17 2TEVA PHARMS USA
18 2WATSON LABS INC
19 2ZYDUS
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01 1SPRAY;NASAL
02 2TABLET; ORAL
03 34TABLET;ORAL
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01 2DISCN
02 31RX
03 4Blank
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01 2CHANTIX
02 1TYRVAYA
03 2VARENICLINE
04 32VARENICLINE TARTRATE
01 30No
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Dosage Strength : EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
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
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