01 12Eli Lilly
02 2Theratechnologies
01 11INJECTABLE;INJECTION
02 2POWDER;SUBCUTANEOUS
03 1SOLUTION;SUBCUTANEOUS
01 14Blank
01 2EGRIFTA
02 1HUMALOG
03 3HUMALOG KWIKPEN
04 1HUMALOG MIX 50/50
05 1HUMALOG MIX 50/50 KWIKPEN
06 1HUMALOG MIX 50/50 PEN
07 1HUMALOG MIX 75/25
08 1HUMALOG MIX 75/25 KWIKPEN
09 1HUMALOG MIX 75/25 PEN
10 1HUMALOG PEN
11 1HUMALOG TEMPO PEN
01 14USA
Regulatory Info :
Registration Country : USA
Brand Name : HUMALOG
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 100 UNITS/ML
Packaging :
Approval Date :
Application Number : 20563
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : HUMALOG PEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 100 UNITS/ML
Packaging :
Approval Date :
Application Number : 20563
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : HUMALOG KWIKPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 100 UNITS/ML
Packaging :
Approval Date :
Application Number : 20563
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : HUMALOG KWIKPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 200UNITS/ML
Packaging :
Approval Date :
Application Number : 20563
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : HUMALOG TEMPO PEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 100UNITS/ML
Packaging :
Approval Date :
Application Number : 20563
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
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
Regulatory Info :
Registration Country : USA
Brand Name : HUMALOG KWIKPEN
Dosage Form : SOLUTION;SUBCUTANEOUS
Dosage Strength : 200 UNITS/ML
Packaging :
Approval Date :
Application Number : 205747
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : EGRIFTA
Dosage Form : POWDER;SUBCUTANEOUS
Dosage Strength : EQ 1MG BASE/VIAL
Packaging :
Approval Date :
Application Number : 22505
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
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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