Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 7Sanofi
02 1Aspen Pharmacare Holdings
03 1ATNAHS PHARMA UK LIMITED
04 2Apotex Inc
05 2Arrow Pharmaceuticals
06 5Clinect
07 1Cosette Pharma
08 3GSK
09 2Generic Health
10 1ODAN LABORATORIES LTD
11 1Padagis
12 2Pharmascience Inc.
13 1RELIANCE FORMULATION PVT. LTD
14 4SOLVAY PHARMA SpA
15 3Sun Pharmaceutical Industries Limited
16 2TEOFARMA Srl
17 2WAGNER PHARMACEUTICALS PTY LTD
01 1INJ
02 1SOLUTION
03 2SUP
04 2SUPPOSITORY
05 8SUPPOSITORY;RECTAL
06 1Suppository
07 3TAB
08 3Tablet
09 10tablet
10 9Blank
01 6DISCN
02 2Deregistered
03 1Generic
04 1Marketed
05 5Originator
06 3Prescription
07 2RX
08 20Blank
01 2APO-Prochlorperazine
02 3COMPAZINE
03 1COMPRO
04 4Difmetre
05 1Mitil
06 1ODAN-PROCHLORPERAZINE
07 1PMS PROCHLORPERAZINE INJ 5MG/ML
08 1PMS-PROCHLORPERAZINE SUPPOSITOIRES 10MG
09 4PROCHLORPERAZINE
10 2PROCHLORPERAZINE-WGR
11 2ProCalm
12 2Prochlorperazine GH
13 11Stemetil
14 1Stemetil 25 mg Suppositories
15 1Stemetil 5 mg Suppositories
16 1Stemetil 1.25% m/v/1ml Injection
17 1Stemetil 5 mg Tablets
18 1Blank
01 13Australia
02 3Canada
03 1India
04 6Italy
05 1Norway
06 6South Africa
07 2Sweden
08 8USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Stemetil
Dosage Form : Suppository
Dosage Strength : 25mg
Packaging :
Approval Date : 04/11/1958
Application Number : 19581104000052
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Mitil
Dosage Form : TAB
Dosage Strength : 5mg
Packaging : 250X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Stemetil
Dosage Form : Tablet
Dosage Strength : 5mg
Packaging :
Approval Date : 04/11/1958
Application Number : 19581104000045
Regulatory Info : Deregistered
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Stemetil 1.25% m/v/1ml Injection
Dosage Form : INJ
Dosage Strength : 1.2% m/v/ml
Packaging : 1X10% m/v/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Stemetil 5 mg Suppositories
Dosage Form : SUP
Dosage Strength : 5mg
Packaging : 5X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Stemetil 25 mg Suppositories
Dosage Form : SUP
Dosage Strength : 25mg
Packaging : 5X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Stemetil
Dosage Form : TAB
Dosage Strength : 5mg
Packaging : 25X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Stemetil 5 mg Tablets
Dosage Form : TAB
Dosage Strength : 5mg
Packaging : 250X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 25MG
Packaging :
Approval Date : 1993-11-24
Application Number : 40058
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 11127
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 11127
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : COMPAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 11127
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : COMPRO
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2000-06-28
Application Number : 40246
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-PROCHLORPERAZINE SUPPOSITOIRES 10MG
Dosage Form : SUPPOSITORY
Dosage Strength : 10MG
Packaging : 10
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS PROCHLORPERAZINE INJ 5MG/ML
Dosage Form : SOLUTION
Dosage Strength : 5MG/ML
Packaging : 10 X 2ML
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2001-07-11
Application Number : 40407
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2001-07-11
Application Number : 40407
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROCHLORPERAZINE
Dosage Form : SUPPOSITORY;RECTAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2001-07-11
Application Number : 40407
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Indomethacin; Caffeine; Prochlorperazine
Brand Name : Difmetre
Dosage Form :
Dosage Strength : 6 Supp
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Indomethacin; Caffeine; Prochlorperazine
Brand Name : Difmetre
Dosage Form :
Dosage Strength : 6 Media Low Dosage
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
