DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2DR REDDYS LABS SA
02 2AJANTA PHARMA LTD
03 2AMNEAL
04 2AUROBINDO PHARMA LTD
05 2BIONPHARMA
06 3CHARTWELL RX
07 5DURAMED PHARMS BARR
08 9GLAXOSMITHKLINE
09 2GLENMARK PHARMS LTD
10 2IVAX SUB TEVA PHARMS
11 2JUBILANT CADISTA
12 2LEADING
13 2NOVITIUM PHARMA
14 2PHARMOBEDIENT
15 2TEVA PHARMS
16 3WATSON LABS
17 2ZYDUS LIFESCIENCES
01 6CAPSULE, EXTENDED RELEASE;ORAL
02 40TABLET;ORAL
01 26DISCN
02 20RX
01 9COMPAZINE
02 3PROCHLORPERAZINE
03 32PROCHLORPERAZINE MALEATE
04 2PROCOMP
01 43No
02 3Yes
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Approval Date : 2025-05-19
Application Number : 217847
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 : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Approval Date : 2025-05-19
Application Number : 217847
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : COMPAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 10571
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : COMPAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 10571
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : COMPAZINE
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Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 1982-01-01
Application Number : 10571
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 10MG BASE
Approval Date : 1982-01-01
Application Number : 11000
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 15MG BASE
Approval Date : 1982-01-01
Application Number : 11000
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 30MG BASE
Approval Date : 1982-01-01
Application Number : 11000
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 75MG BASE
Approval Date : 1982-01-01
Application Number : 11000
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 10MG BASE
Approval Date : 1999-10-06
Application Number : 21019
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
