Home NDC 0002-7512-99 Humalog
Product NDC 0002-7512
Requested package NDC 0002-7512-99
11-digit product format 000027512
Labeler code 0002
Product ID 0002-7512_b2e34993-838d-4e33-bf5e-c9fa4920a536
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Insulin lispro
Dosage form INJECTION, SUSPENSION
Route SUBCUTANEOUS
Labeler Eli Lilly and Company
Application BLA021018
Marketing category BLA
Marketing start 1999-12-22
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0002-7512-01 Humalog Mix50/50 10 mL in 1 VIAL, MULTI-DOSE INJECTION, SUSPENSION 10 54 0002-7512-01 Humalog Mix50/50 1 in 1 CARTON INJECTION, SUSPENSION 1 54 0002-7512-99 Humalog Mix50/50 1 in 1 CARTON INJECTION, SUSPENSION 1 54 0002-7512-99 Humalog Mix50/50 10 mL in 1 VIAL, MULTI-DOSE INJECTION, SUSPENSION 10 54
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Insulin lispro ACTIVE INGREDIENT GFX7QIS1II HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Insulin lispro ACTIVE MOIETY GFX7QIS1II HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Glycerin INACTIVE INGREDIENT PDC6A3C0OX HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Hydrochloric acid INACTIVE INGREDIENT QTT17582CB HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Metacresol INACTIVE INGREDIENT GGO4Y809LO HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Phenol INACTIVE INGREDIENT 339NCG44TV HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Protamine sulfate INACTIVE INGREDIENT 0DE9724IHC HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Sodium hydroxide INACTIVE INGREDIENT 55X04QC32I HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Sodium Phosphate, Dibasic INACTIVE INGREDIENT GR686LBA74 HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Water INACTIVE INGREDIENT 059QF0KO0R HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32 Zinc INACTIVE INGREDIENT J41CSQ7QDS HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 32
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0002-7512 HUMALOG MIX50/50 (INSULIN LISPRO) INJECTION, SUSPENSION HUMALOG MIX50/50 KWIKPEN (INSULIN LISPRO) INJECTION, SUSPENSION [ELI LILLY AND COMPANY] 53 Legacy NDC, 4 package rows 20241215_b34cd3ff-d0af-4852-b4ef-2a8b4a93aeae.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 021018 Humalog Mix 50/50 insulin lispro protamine and insulin lispro 351(a) Disc 2026-07-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0002-7512-99 00002751299 1 VIAL, MULTI-DOSE in 1 CARTON (0002-7512-99) > 10 mL in 1 VIAL, MULTI-DOSE 2006-10-19 0000-00-00 Yes No Current