NDC 0002-8799-01 - Humalog
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0002-8799
- Requested NDC
- 0002-8799-01
- Package NDCs from labels
- 0002-8799-01, 0002-8799-59
- Manufacturer
- Eli Lilly and Company
- Effective date
- 2026-06-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Humalog - Eli Lilly and Company | Eli Lilly and Company | 2026-06-16 | HUMAN PRESCRIPTION DRUG LABEL |
| HUMALOG - A-S Medication Solutions | A-S Medication Solutions | 2025-04-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Humalog KwikPen - A-S Medication Solutions | A-S Medication Solutions | 2024-01-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Humalog KwikPen - REMEDYREPACK INC. | REMEDYREPACK INC. | 2022-01-26 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0002-8799-01 | HumalogKwikPen | 3 mL in 1 SYRINGE | INJECTION, SOLUTION | 3 | 86 | |
| 0002-8799-59 | HumalogKwikPen | 5 in 1 CARTON | INJECTION, SOLUTION | 5 | 86 | |
| 0002-8799-61 | HumalogKwikPen | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | 86 | |
| 0002-8799-61 | HumalogKwikPen | 3 mL in 1 SYRINGE | INJECTION, SOLUTION | 3 | 86 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0002-8799 | HUMALOG (INSULIN LISPRO) INJECTION, SOLUTION HUMALOG KWIKPEN (INSULIN LISPRO) INJECTION, SOLUTION HUMALOG JUNIOR KWIKPEN (INSULIN LISPRO) INJECTION, SOLUTION HUMALOG TEMPO PEN (INSULIN LISPRO) INJECTION, SOLUTION STERILE DILUENT (DILUENT) INJECTION, SOLUTION HUMALOG TEMPO PEN (INSULIN LISPRO) INJECTION, SOLUTION [ELI LILLY AND COMPANY] | 84 | Current NDC, Legacy NDC, 4 package rows | 20250523_c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0002-8799-01 | ML - Milliliter | 0002-8799 | 57778c30-09bb-4973-bf6e-a588ce5e9590 | 1 | 2012-07-24 |
| 0002-8799-59 | ML - Milliliter | 0002-8799 | 99c49b1b-fb95-492e-b6f8-9f944d3d0c51 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Diathesis V 1 | GINKGO BILOBA, PANCREAS (SUIS), SPLEEN (SUIS), STOMACH (SUIS), GERMANIUM SESQUIOXIDE, CUPRUM METALLICUM, CYSTEINUM, ZINCUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, NATRUM OXALACETICUM | BioActive Nutritional, Inc. | 58a16fcf-b05f-41a9-a580-41da6300ac7f | 2016-11-04 | Warnings | J41CSQ7QDS |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.