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01 12Eli Lilly

02 2Theratechnologies

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PharmaCompass

01

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100 UNITS/ML

Packaging :

Approval Date :

Application Number : 20563

Regulatory Info :

Registration Country : USA

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02

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG PEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100 UNITS/ML

Packaging :

Approval Date :

Application Number : 20563

Regulatory Info :

Registration Country : USA

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03

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG KWIKPEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100 UNITS/ML

Packaging :

Approval Date :

Application Number : 20563

Regulatory Info :

Registration Country : USA

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04

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG KWIKPEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200UNITS/ML

Packaging :

Approval Date :

Application Number : 20563

Regulatory Info :

Registration Country : USA

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05

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG TEMPO PEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100UNITS/ML

Packaging :

Approval Date :

Application Number : 20563

Regulatory Info :

Registration Country : USA

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06

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO PROTAMINE RECOMBINANT; INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG MIX 75/25

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 75 UNITS/ML;25 UNITS/ML

Packaging :

Approval Date :

Application Number : 21017

Regulatory Info :

Registration Country : USA

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07

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO PROTAMINE RECOMBINANT; INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG MIX 75/25 KWIKPEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 75 UNITS/ML;25 UNITS/ML

Packaging :

Approval Date :

Application Number : 21017

Regulatory Info :

Registration Country : USA

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08

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO PROTAMINE RECOMBINANT; INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG MIX 75/25 PEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 75 UNITS/ML;25 UNITS/ML

Packaging :

Approval Date :

Application Number : 21017

Regulatory Info :

Registration Country : USA

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09

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO PROTAMINE RECOMBINANT; INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG MIX 50/50

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50 UNITS/ML;50 UNITS/ML

Packaging :

Approval Date :

Application Number : 21018

Regulatory Info :

Registration Country : USA

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10

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO PROTAMINE RECOMBINANT; INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG MIX 50/50 KWIKPEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50 UNITS/ML;50 UNITS/ML

Packaging :

Approval Date :

Application Number : 21018

Regulatory Info :

Registration Country : USA

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11

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO PROTAMINE RECOMBINANT; INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG MIX 50/50 PEN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50 UNITS/ML;50 UNITS/ML

Packaging :

Approval Date :

Application Number : 21018

Regulatory Info :

Registration Country : USA

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12

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

INSULIN LISPRO RECOMBINANT

Brand Name : HUMALOG KWIKPEN

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 200 UNITS/ML

Packaging :

Approval Date :

Application Number : 205747

Regulatory Info :

Registration Country : USA

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13

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

TESAMORELIN ACETATE

Brand Name : EGRIFTA

Dosage Form : POWDER;SUBCUTANEOUS

Dosage Strength : EQ 1MG BASE/VIAL

Packaging :

Approval Date :

Application Number : 22505

Regulatory Info :

Registration Country : USA

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14

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

TESAMORELIN ACETATE

Brand Name : EGRIFTA

Dosage Form : POWDER;SUBCUTANEOUS

Dosage Strength : EQ 2MG BASE/VIAL

Packaging :

Approval Date :

Application Number : 22505

Regulatory Info :

Registration Country : USA

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