Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 2GRANULES
02 2MANKIND PHARMA
03 2ACTAVIS TOTOWA
04 1AJANTA PHARMA LTD
05 1ALEMBIC
06 2AMNEAL PHARMS
07 1ANNORA PHARMA
08 1ASPIRO
09 3AUROBINDO PHARMA LTD
10 3BAXTER HLTHCARE CORP
11 1BE PHARMS
12 1CIPLA
13 1DEXCEL
14 2DR REDDYS LABS LTD
15 1EPIC PHARMA LLC
16 1EUGIA PHARMA
17 1FRESENIUS KABI USA
18 1GLAND
19 2GRAVITI PHARMS
20 1HANGZHOU ZHONGMEI
21 2HETERO LABS LTD V
22 1HIKMA
23 1INGENUS PHARMS LLC
24 2JUBILANT GENERICS
25 1KNACK
26 1L PERRIGO CO
27 2LANNETT CO INC
28 2MACLEODS PHARMS LTD
29 1MEITHEAL
30 2MYLAN PHARMS INC
31 1NORVIUM BIOSCIENCE
32 2ORBION PHARMS
33 2RUBICON
34 1SANDOZ
35 4SUN PHARM
36 2SUN PHARM INDS LTD
37 2TEVA
38 1TEVA PARENTERAL
39 2TORRENT PHARMS
40 2WOCKHARDT BIO AG
41 4WYETH PHARMS
01 7FOR SUSPENSION, DELAYED RELEASE;ORAL
02 1INJECTABLE; INJECTION
03 13INJECTABLE;INTRAVENOUS
04 2POWDER;INTRAVENOUS
05 3SOLUTION;INTRAVENOUS
06 42TABLET, DELAYED RELEASE;ORAL
01 17DISCN
02 50RX
03 1Blank
01 61PANTOPRAZOLE SODIUM
02 3PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE
03 3PROTONIX
04 1PROTONIX IV
01 59No
02 8Yes
03 1Blank
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 : PANTOPRAZOLE SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 20MG BASE
Approval Date : 2023-12-11
Application Number : 217282
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : PANTOPRAZOLE SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 40MG BASE
Approval Date : 2022-07-26
Application Number : 215880
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 : PANTOPRAZOLE SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 40MG BASE
Approval Date : 2023-12-11
Application Number : 217282
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code :
Brand Name : PANTOPRAZOLE SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 20MG BASE
Approval Date : 2024-04-25
Application Number : 215880
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
Brand Name : PANTOPRAZOLE SODIUM
Dosage Form : INJECTABLE; INJECTION
Dosage Strength : 40MG
Approval Date :
Application Number : 22226
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code :
Brand Name : PANTOPRAZOLE SODIUM
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 20MG BASE
Approval Date : 2007-08-02
Application Number : 77056
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Brand Name : PROTONIX
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 40MG BASE
Approval Date : 2000-02-02
Application Number : 20987
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : PROTONIX
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : EQ 20MG BASE
Approval Date : 2001-06-12
Application Number : 20987
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AP
Brand Name : PROTONIX IV
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : EQ 40MG BASE/VIAL
Approval Date : 2001-03-22
Application Number : 20988
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AB
Brand Name : PROTONIX
Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL
Dosage Strength : EQ 40MG BASE
Approval Date : 2007-11-14
Application Number : 22020
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
