Humalog

Product NDC
70518-1388
11-digit product format
705181388
Labeler code
70518
Product ID
70518-1388_d68305a6-d86a-3f85-e053-2995a90a6f21
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Insulin lispro
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS; SUBCUTANEOUS
Labeler
REMEDYREPACK INC.
Application
BLA020563
Marketing category
BLA
Marketing start
2018-08-27
Marketing end
0000-00-00
Substance
INSULIN LISPRO
Active strength
100 [iU]/mL
Pharmacologic classes
Insulin Analog [EPC], Insulin [Chemical/Ingredient]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-1388-02020-11-18C16284748780-19d75b9d0-bc20-f424-e053-dadaa90a57ce7ea5ac79-79a7-442c-9c34-3b6477367928
70518-1388-02020-01-31C16284748780-19d75b9d0-bc20-f424-e053-dadaa90a57ce7ea5ac79-79a7-442c-9c34-3b6477367928

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-1388-0705181388001 VIAL in 1 CARTON (70518-1388-0) > 3 mL in 1 VIAL1 vial2018-08-270000-00-00NoNoCurrent