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01 5ESTRADIOL

02 1SUFENTANIL CITRATE

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PharmaCompass

01

Brand Name : DIVIGEL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIVIGEL

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Pharmtech & Ingredients
Not Confirmed

Vertical Pharmaceuticals

Dosage Form : GEL;TRANSDERMAL

Brand Name : DIVIGEL

Dosage Strength : 0.1% (0.25GM/PACKET)

Packaging :

Approval Date : 2007-06-04

Application Number : 22038

Regulatory Info : RX

Registration Country : USA

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02

Brand Name : DIVIGEL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIVIGEL

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Pharmtech & Ingredients
Not Confirmed

Vertical Pharmaceuticals

Dosage Form : GEL;TRANSDERMAL

Brand Name : DIVIGEL

Dosage Strength : 0.1% (0.5GM/PACKET)

Packaging :

Approval Date : 2007-06-04

Application Number : 22038

Regulatory Info : RX

Registration Country : USA

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03

Brand Name : DIVIGEL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIVIGEL

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Pharmtech & Ingredients
Not Confirmed

Vertical Pharmaceuticals

Dosage Form : GEL;TRANSDERMAL

Brand Name : DIVIGEL

Dosage Strength : 0.1% (1GM/PACKET)

Packaging :

Approval Date : 2007-06-04

Application Number : 22038

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : DIVIGEL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIVIGEL

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Pharmtech & Ingredients
Not Confirmed

Vertical Pharmaceuticals

Dosage Form : GEL;TRANSDERMAL

Brand Name : DIVIGEL

Dosage Strength : 0.1% (0.75GM/PACKET)

Packaging :

Approval Date : 2018-08-17

Application Number : 22038

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : DIVIGEL

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIVIGEL

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Pharmtech & Ingredients
Not Confirmed

Vertical Pharmaceuticals

Dosage Form : GEL;TRANSDERMAL

Brand Name : DIVIGEL

Dosage Strength : 0.1% (1.25GM/PACKET)

Packaging :

Approval Date : 2019-12-12

Application Number : 22038

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : DSUVIA

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DSUVIA

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Pharmtech & Ingredients
Not Confirmed

Vertical Pharmaceuticals

Dosage Form : TABLET;SUBLINGUAL

Brand Name : DSUVIA

Dosage Strength : EQ 0.03MG BASE

Packaging :

Approval Date : 2018-11-02

Application Number : 209128

Regulatory Info : RX

Registration Country : USA

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