01 2AAIPharma Services Corp.
02 3Actavis Inc
03 1Adcock Ingram
04 2Ajanta Pharma Limited
05 2Amneal Pharmaceuticals
06 2Bionpharma
07 3Chartwell Pharmaceuticals llc
08 5DURAMED PHARMS BARR
09 2DelNova Healthcare
10 9GSK
11 2Glenmark Pharmaceuticals
12 1Halewood Laboratories Pvt. Ltd
13 2IVAX Pharmaceuticals Inc
14 1Ipca Laboratories
15 2Jubilant Cadista Pharmaceuticals
16 1Kusum Healthcare Pvt Ltd
17 2Leading Pharma, LLC
18 2NORVIUM BIOSCIENCE
19 2Novitium Pharma LLC
20 2Pharmascience Inc.
21 2Teva Pharmaceutical Industries
22 2Zydus Lifesciences
01 6CAPSULE, EXTENDED RELEASE;ORAL
02 1TAB
03 6TABLET
04 1TABLET
05 36TABLET;ORAL
06 2Tablet
01 26DISCN
02 3Generic
03 1Generic CTD, BE
04 4Prescription
05 16RX
06 2Blank
01 9COMPAZINE
02 1PMS-PROCHLORPERAZINE TAB 10MG
03 1PMS-PROCHLORPERAZINE TAB 5MG
04 2PROCHLORAZINE
05 3PROCHLORPERAZINE
06 28PROCHLORPERAZINE MALEATE
07 2PROCOMP
08 1Scripto-Metic 5 mg
09 1VERTINEX
10 4Blank
01 4Canada
02 5India
03 1South Africa
04 42USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 85178
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 85579
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 85580
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1996-07-19
Application Number : 40101
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1996-07-19
Application Number : 40101
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1996-07-19
Application Number : 40101
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1997-05-01
Application Number : 40207
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1997-05-01
Application Number : 40207
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1987-01-20
Application Number : 89484
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1987-01-20
Application Number : 89485
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1987-01-20
Application Number : 89486
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-01-01
Application Number : 10571
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-01-01
Application Number : 10571
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-01-01
Application Number : 10571
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 11000
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 11000
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 30MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 11000
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 11000
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1999-10-06
Application Number : 21019
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 1999-10-06
Application Number : 21019
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1998-01-20
Application Number : 40162
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1998-01-20
Application Number : 40162
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PROCOMP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1998-02-27
Application Number : 40268
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PROCOMP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1998-02-27
Application Number : 40268
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2022-06-13
Application Number : 216202
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2022-06-13
Application Number : 216202
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1996-07-11
Application Number : 40120
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1996-07-11
Application Number : 40120
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1996-10-28
Application Number : 40185
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE MALEATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1996-10-28
Application Number : 40185
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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