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01 3A&M Therapy

02 4Actavis Inc

03 2Amdipharm Mercury Company Limited

04 2Avet Pharmaceuticals

05 3Novartis Pharmaceuticals Corporation

06 3Rising Pharmaceuticals Inc

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PharmaCompass

01

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1988-01-14

Application Number : 72129

Regulatory Info : DISCN

Registration Country : USA

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02

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1988-01-14

Application Number : 72130

Regulatory Info : DISCN

Registration Country : USA

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03

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1988-01-14

Application Number : 72131

Regulatory Info : DISCN

Registration Country : USA

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04

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1987-12-30

Application Number : 71943

Regulatory Info : DISCN

Registration Country : USA

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05

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1987-12-30

Application Number : 71944

Regulatory Info : DISCN

Registration Country : USA

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06

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1987-12-30

Application Number : 71945

Regulatory Info : DISCN

Registration Country : USA

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07

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1988-06-01

Application Number : 72164

Regulatory Info : DISCN

Registration Country : USA

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08

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

Maprotiline Hydrochloride

Brand Name : Ludiomil

Dosage Form : Tablet

Dosage Strength : 75MG

Packaging :

Approval Date : 1982-01-01

Application Number : 55706

Regulatory Info : Authorized

Registration Country : Spain

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09

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

Maprotiline Hydrochloride

Brand Name : Ludiomil

Dosage Form : Tablet

Dosage Strength : 25MG

Packaging :

Approval Date : 1973-10-01

Application Number : 51648

Regulatory Info : Authorized

Registration Country : Spain

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10

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1988-06-01

Application Number : 72162

Regulatory Info : DISCN

Registration Country : USA

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11

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1988-06-01

Application Number : 72163

Regulatory Info : DISCN

Registration Country : USA

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12

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : LUDIOMIL

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1982-01-01

Application Number : 17543

Regulatory Info : DISCN

Registration Country : USA

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13

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : LUDIOMIL

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 17543

Regulatory Info : DISCN

Registration Country : USA

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14

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : LUDIOMIL

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1982-09-30

Application Number : 17543

Regulatory Info : DISCN

Registration Country : USA

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15

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1988-10-03

Application Number : 72285

Regulatory Info : DISCN

Registration Country : USA

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16

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Packaging :

Approval Date : 1988-10-03

Application Number : 72285

Regulatory Info : DISCN

Registration Country : USA

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17

BioJapan
Not Confirmed
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BioJapan
Not Confirmed

MAPROTILINE HYDROCHLORIDE

Brand Name : MAPROTILINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG

Packaging :

Approval Date : 1988-10-03

Application Number : 72285

Regulatory Info : DISCN

Registration Country : USA

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