Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 1Ampoule
02 1CONCENTRATE;ORAL
03 1Chewable Tablet
04 1Drop
05 2INJ
06 20INJECTABLE;INJECTION
07 1INJECTION
08 1Injectable And Infusion Solution
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10 1Injectable; Injection
11 3Injection
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15 1Oral Solution Powder
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29 14Tablet
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01 1Adco Contromet Syrup
02 1Adco Contromet Tablet
03 1Adco Metoclopramide 10Mg/2Ml
04 2CLOPRA
05 1CLOPRA-"YELLOW"
06 1GIMOTI
07 1MAR-METOCLOPRAMIDE
08 1MAXOLON
09 1METOCLOPRAMIDE
10 1METOCLOPRAMIDE HCL
11 61METOCLOPRAMIDE HYDROCHLORIDE
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13 78USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Deregistered
Registration Country : Sweden
Acetylsalicylate-DL-Lysine; Metoclopramide Hydrochloride Monohydrate
Brand Name : Migpriv
Dosage Form : Oral Solution Powder
Dosage Strength : 900mg;10mg
Packaging :
Approval Date : 1998-08-28
Application Number : 19980828000018
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info :
Registration Country : India
Brand Name : Metoclopramide Hydrochloride
Dosage Form : Tablet
Dosage Strength : 10mg
Packaging : Pack Size 10x10
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : METOCLOPRAMIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1985-10-17
Application Number : 70581
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Metoclopramida Pensa
Dosage Form : Oral Solution
Dosage Strength : 1MG
Packaging :
Approval Date : 2007-09-19
Application Number : 69265
Regulatory Info : Authorized
Registration Country : Spain
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Primperan
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date : 1965-07-01
Application Number : 41446
Regulatory Info : Authorized
Registration Country : Spain
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Primperan
Dosage Form : Injectable Solution
Dosage Strength : 10MG
Packaging :
Approval Date : 1964-12-01
Application Number : 40256
Regulatory Info : Authorized
Registration Country : Spain
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Primperan
Dosage Form : Solution
Dosage Strength : 1MG
Packaging :
Approval Date : 1964-12-01
Application Number : 40257
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info :
Registration Country : India
Brand Name : Metoclopramide Hydrochloride
Dosage Form : Injection
Dosage Strength : 5mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
Brand Name : METOCLOPRAMIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2006-08-28
Application Number : 77878
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : METOCLOPRAMIDE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2006-08-28
Application Number : 77878
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : Metoclopramide Hydrochloride
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Metoclopramide Hydrochloride
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REGLAN
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1983-03-25
Application Number : 18821
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : REGLAN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 17854
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : REGLAN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 1987-05-05
Application Number : 17854
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REGLAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17862
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REGLAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1987-05-28
Application Number : 17862
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REGLAN ODT
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2005-06-10
Application Number : 21793
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REGLAN ODT
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2005-06-10
Application Number : 21793
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : METOZOLV ODT
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-09-04
Application Number : 22246
Regulatory Info : DISCN
Registration Country : USA
