Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 3GRANULES
02 2ABON PHARMS LLC
03 1ADAPTIS
04 4AJANTA PHARMA LTD
05 3ALEMBIC
06 5ALEMBIC PHARMS LTD
07 4ALKEM LABS LTD
08 5AMNEAL PHARMS
09 3ANCHEN PHARMS
10 3ANNORA PHARMA
11 2APPCO
12 4ASCENT PHARMS INC
13 5AUROBINDO PHARMA
14 3AUROBINDO PHARMA LTD
15 8CADILA PHARMS LTD
16 5CHARTWELL RX
17 2DEXCEL
18 8DR REDDYS LABS LTD
19 5HERITAGE
20 3IMPAX LABS
21 3INVENTIA HLTHCARE
22 3MACLEODS PHARMS LTD
23 3MEDICAP LABS
24 2MPP PHARMA
25 3NOSTRUM PHARMS LLC
26 3ORBION PHARMS
27 4OSMOTICA PHARM US
28 8PHARMOBEDIENT
29 5PLIVA HRVATSKA DOO
30 5PRINSTON INC
31 3SCIEGEN PHARMS INC
32 4SUN PHARM
33 5SUN PHARM INDS INC
34 2SWISS PHARM
35 8TEVA
36 7TORRENT
37 4UNIQUE
38 4UPJOHN
39 3VALEANT PHARMS NORTH
40 6WYETH PHARMS INC
41 5YAOPHARMA CO LTD
42 3YICHANG HUMANWELL
43 4ZYDUS PHARMS
44 5ZYDUS PHARMS USA
45 3ZYDUS PHARMS USA INC
01 3CAPSULE, EXTENDED RELEASE; ORAL
02 58CAPSULE, EXTENDED RELEASE;ORAL
03 46TABLET, EXTENDED RELEASE;ORAL
04 76TABLET;ORAL
01 57DISCN
02 123RX
03 3Blank
01 6EFFEXOR
02 4EFFEXOR XR
03 173VENLAFAXINE HYDROCHLORIDE
01 167No
02 13Yes
03 3Blank
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
RLD : No
TE Code : AB
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 37.5MG BASE
Approval Date : 2023-05-18
Application Number : 217390
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
RLD : No
TE Code : AB
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 75MG BASE
Approval Date : 2023-05-18
Application Number : 217390
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
RLD : No
TE Code : AB
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 150MG BASE
Approval Date : 2023-05-18
Application Number : 217390
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : EFFEXOR XR
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 37.5MG BASE
Approval Date : 1997-10-20
Application Number : 20699
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : EFFEXOR
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-28
Application Number : 20151
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : EFFEXOR
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-28
Application Number : 20151
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : EFFEXOR
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-28
Application Number : 20151
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : EFFEXOR
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-28
Application Number : 20151
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : EFFEXOR
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-28
Application Number : 20151
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : EFFEXOR
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-12-28
Application Number : 20151
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
