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01 5ESTRADIOL

02 1SUFENTANIL CITRATE

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PharmaCompass

01

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
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Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Vertical Pharmaceuticals

Dosage Form : GEL; TRANSDERMAL

Proprietary Name : DIVIGEL

Dosage Strength : 0.1% (0.25GM/PACKET)

Approval Date : 2007-06-04

Application Number : 22038

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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02

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Vertical Pharmaceuticals

Dosage Form : GEL; TRANSDERMAL

Proprietary Name : DIVIGEL

Dosage Strength : 0.1% (0.5GM/PACKET)

Approval Date : 2007-06-04

Application Number : 22038

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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03

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Vertical Pharmaceuticals

Dosage Form : GEL; TRANSDERMAL

Proprietary Name : DIVIGEL

Dosage Strength : 0.1% (1GM/PACKET)

Approval Date : 2007-06-04

Application Number : 22038

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Vertical Pharmaceuticals

Dosage Form : GEL; TRANSDERMAL

Proprietary Name : DIVIGEL

Dosage Strength : 0.1% (0.75GM/PACKET)

Approval Date : 2018-08-17

Application Number : 22038

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Brand Name : DIVIGEL

Medlab Asia & Asia Health
Not Confirmed
arrow

Vertical Pharmaceuticals

Dosage Form : GEL; TRANSDERMAL

Proprietary Name : DIVIGEL

Dosage Strength : 0.1% (1.25GM/PACKET)

Approval Date : 2019-12-12

Application Number : 22038

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

Brand Name : DSUVIA

Medlab Asia & Asia Health
Not Confirmed
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Brand Name : DSUVIA

Medlab Asia & Asia Health
Not Confirmed
arrow

Vertical Pharmaceuticals

Dosage Form : TABLET; SUBLINGUAL

Proprietary Name : DSUVIA

Dosage Strength : EQ 0.03MG BASE

Approval Date : 2018-11-02

Application Number : 209128

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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