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 4AJANTA PHARMA LTD
04 3ALEMBIC
05 5ALEMBIC PHARMS LTD
06 4ALKEM LABS LTD
07 5AMNEAL PHARMS
08 3ANCHEN PHARMS
09 3ANNORA PHARMA
10 2APPCO
11 4ASCENT PHARMS INC
12 5AUROBINDO PHARMA
13 3AUROBINDO PHARMA LTD
14 8CADILA PHARMS LTD
15 5CHARTWELL RX
16 3DEXCEL
17 8DR REDDYS LABS LTD
18 5HERITAGE
19 3IMPAX LABS
20 3INTELLIPHARMACEUTICS
21 3INVENTIA HLTHCARE
22 3MACLEODS PHARMS LTD
23 8NORVIUM BIOSCIENCE
24 2NOSTRUM LABS INC
25 3NOSTRUM PHARMS LLC
26 3ORBION PHARMS
27 4OSMOTICA PHARM US
28 5PLIVA HRVATSKA DOO
29 5PRINSTON INC
30 4SUN PHARM
31 5SUN PHARM INDS INC
32 2SWISS PHARM
33 8TEVA
34 7TORRENT
35 4UNIQUE
36 4UPJOHN
37 3VALEANT PHARMS NORTH
38 3WOCKHARDT BIO AG
39 6WYETH PHARMS INC
40 5YAOPHARMA CO LTD
41 3YICHANG HUMANWELL
42 4ZYDUS PHARMS
43 5ZYDUS PHARMS USA
44 3ZYDUS PHARMS USA INC
01 3CAPSULE, EXTENDED RELEASE; ORAL
02 58CAPSULE, EXTENDED RELEASE;ORAL
03 46TABLET, EXTENDED RELEASE;ORAL
04 76TABLET;ORAL
01 53DISCN
02 127RX
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 :
