Novolin - 0169-1837-11 - (Human Insulin)

Alphabetical Index


Drug Information of Novolin

Product NDC: 0169-1837
Proprietary Name: Novolin
Non Proprietary Name: Human Insulin
Active Ingredient(s): 100    [USP'U]/mL & nbsp;   Human Insulin
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Novolin

Product NDC: 0169-1837
Labeler Name: Novo Nordisk
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019991
Marketing Category: NDA
Start Marketing Date: 19910625

Package Information of Novolin

Package NDC: 0169-1837-11
Package Description: 1 VIAL in 1 CARTON (0169-1837-11) > 10 mL in 1 VIAL

NDC Information of Novolin

NDC Code 0169-1837-11
Proprietary Name Novolin
Package Description 1 VIAL in 1 CARTON (0169-1837-11) > 10 mL in 1 VIAL
Product NDC 0169-1837
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Human Insulin
Dosage Form Name INJECTION, SUSPENSION
Route Name SUBCUTANEOUS
Start Marketing Date 19910625
Marketing Category Name NDA
Labeler Name Novo Nordisk
Substance Name INSULIN HUMAN
Strength Number 100
Strength Unit [USP'U]/mL
Pharmaceutical Classes

Complete Information of Novolin


General Information