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01 2A&M Therapy

02 2ANI Pharmaceuticals Inc

03 4Actavis Inc

04 2Barr Laboratories

05 2Chartwell Pharmaceuticals llc

06 2Menarini

07 1PHARMAFAR Srl

08 2Par Pharmaceutical

09 2Pfizer Inc

10 2Quantum Pharma

11 2USL PHARMA

12 2VITARINE

13 2Viatris

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PharmaCompass

01

Simposio AFI
Not Confirmed
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Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1987-02-10

Application Number : 71362

Regulatory Info : DISCN

Registration Country : USA

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02

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1987-02-10

Application Number : 71363

Regulatory Info : DISCN

Registration Country : USA

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03

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1986-11-25

Application Number : 70400

Regulatory Info : DISCN

Registration Country : USA

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04

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1986-11-25

Application Number : 70401

Regulatory Info : DISCN

Registration Country : USA

blank

05

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1987-08-11

Application Number : 71640

Regulatory Info : DISCN

Registration Country : USA

blank

06

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1987-08-11

Application Number : 71641

Regulatory Info : DISCN

Registration Country : USA

blank

07

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1987-04-15

Application Number : 71469

Regulatory Info : DISCN

Registration Country : USA

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08

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1987-04-15

Application Number : 71469

Regulatory Info : DISCN

Registration Country : USA

blank

09

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1988-03-10

Application Number : 72077

Regulatory Info : DISCN

Registration Country : USA

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10

Simposio AFI
Not Confirmed
arrow
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Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1988-03-10

Application Number : 72078

Regulatory Info : DISCN

Registration Country : USA

blank

11

Simposio AFI
Not Confirmed
arrow
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Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOMEN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 18006

Regulatory Info : DISCN

Registration Country : USA

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12

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOMEN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 18006

Regulatory Info : DISCN

Registration Country : USA

blank

13

Simposio AFI
Not Confirmed
arrow
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Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1987-07-14

Application Number : 71380

Regulatory Info : DISCN

Registration Country : USA

blank

14

Simposio AFI
Not Confirmed
arrow
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Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1987-07-14

Application Number : 71381

Regulatory Info : DISCN

Registration Country : USA

blank

15

USL PHARMA

United Kingdom
Simposio AFI
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1988-03-25

Application Number : 71007

Regulatory Info : DISCN

Registration Country : USA

blank

16

USL PHARMA

United Kingdom
Simposio AFI
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1988-03-25

Application Number : 71008

Regulatory Info : DISCN

Registration Country : USA

blank

17

Simposio AFI
Not Confirmed
arrow
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Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1986-09-03

Application Number : 71081

Regulatory Info : RX

Registration Country : USA

blank

18

Simposio AFI
Not Confirmed
arrow
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1986-09-03

Application Number : 71081

Regulatory Info : RX

Registration Country : USA

blank

19

VITARINE

Country
Simposio AFI
Not Confirmed
arrow

VITARINE

Country
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 1988-06-15

Application Number : 71684

Regulatory Info : DISCN

Registration Country : USA

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20

VITARINE

Country
Simposio AFI
Not Confirmed
arrow

VITARINE

Country
arrow
Simposio AFI
Not Confirmed

MECLOFENAMATE SODIUM

Brand Name : MECLOFENAMATE SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Packaging :

Approval Date : 1988-06-15

Application Number : 71710

Regulatory Info : DISCN

Registration Country : USA

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