Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 3GRANULES
02 4AJANTA PHARMA LTD
03 3ALEMBIC
04 5ALEMBIC PHARMS LTD
05 4ALKEM LABS LTD
06 5AMNEAL PHARMS
07 3ANCHEN PHARMS
08 3ANNORA PHARMA
09 2APPCO
10 4ASCENT PHARMS INC
11 5AUROBINDO PHARMA
12 3AUROBINDO PHARMA LTD
13 8CADILA PHARMS LTD
14 5CHARTWELL RX
15 3DEXCEL
16 8DR REDDYS LABS LTD
17 5HERITAGE
18 3IMPAX LABS
19 3INTELLIPHARMACEUTICS
20 3INVENTIA HLTHCARE
21 3MACLEODS PHARMS LTD
22 8NORVIUM BIOSCIENCE
23 2NOSTRUM LABS INC
24 3NOSTRUM PHARMS LLC
25 3ORBION PHARMS
26 4OSMOTICA PHARM US
27 5PLIVA HRVATSKA DOO
28 5PRINSTON INC
29 4SUN PHARM
30 5SUN PHARM INDS INC
31 2SWISS PHARM
32 8TEVA
33 3TORRENT
34 4UNIQUE
35 4UPJOHN
36 3VALEANT PHARMS NORTH
37 3WOCKHARDT BIO AG
38 6WYETH PHARMS INC
39 5YAOPHARMA CO LTD
40 3YICHANG HUMANWELL
41 4ZYDUS PHARMS
42 5ZYDUS PHARMS USA
43 3ZYDUS PHARMS USA INC
01 3CAPSULE, EXTENDED RELEASE; ORAL
02 58CAPSULE, EXTENDED RELEASE;ORAL
03 40TABLET, EXTENDED RELEASE;ORAL
04 76TABLET;ORAL
01 49DISCN
02 125RX
03 3Blank
01 6EFFEXOR
02 4EFFEXOR XR
03 167VENLAFAXINE HYDROCHLORIDE
01 161No
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 :
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