Home > National Drug Code (NDC) > Humulin 70/30

Humulin 70/30 - 52125-415-01 - (Insulin human)

Alphabetical Index


Drug Information of Humulin 70/30

Product NDC: 52125-415
Proprietary Name: Humulin 70/30
Non Proprietary Name: Insulin human
Active Ingredient(s): 100    [iU]/mL & nbsp;   Insulin human
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Humulin 70/30

Product NDC: 52125-415
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019717
Marketing Category: NDA
Start Marketing Date: 20130612

Package Information of Humulin 70/30

Package NDC: 52125-415-01
Package Description: 10 mL in 1 VIAL (52125-415-01)

NDC Information of Humulin 70/30

NDC Code 52125-415-01
Proprietary Name Humulin 70/30
Package Description 10 mL in 1 VIAL (52125-415-01)
Product NDC 52125-415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Insulin human
Dosage Form Name INJECTION, SUSPENSION
Route Name SUBCUTANEOUS
Start Marketing Date 20130612
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name INSULIN HUMAN
Strength Number 100
Strength Unit [iU]/mL
Pharmaceutical Classes Insulin [Chemical/Ingredient],Insulin [EPC]

Complete Information of Humulin 70/30


General Information