Humulin - 0002-8215-17 - (Insulin human)

Alphabetical Index


Drug Information of Humulin

Product NDC: 0002-8215
Proprietary Name: Humulin
Non Proprietary Name: Insulin human
Active Ingredient(s): 100    [iU]/mL & nbsp;   Insulin human
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Humulin

Product NDC: 0002-8215
Labeler Name: Eli Lilly and Company
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA018780
Marketing Category: NDA
Start Marketing Date: 19830627

Package Information of Humulin

Package NDC: 0002-8215-17
Package Description: 1 VIAL in 1 CARTON (0002-8215-17) > 3 mL in 1 VIAL

NDC Information of Humulin

NDC Code 0002-8215-17
Proprietary Name Humulin
Package Description 1 VIAL in 1 CARTON (0002-8215-17) > 3 mL in 1 VIAL
Product NDC 0002-8215
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Insulin human
Dosage Form Name INJECTION, SOLUTION
Route Name PARENTERAL
Start Marketing Date 19830627
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name INSULIN HUMAN
Strength Number 100
Strength Unit [iU]/mL
Pharmaceutical Classes

Complete Information of Humulin


General Information