NDC 0002-7752-01 - Insulin Lispro
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
- 0002-7752
- Requested NDC
- 0002-7752-01
- Package NDCs from labels
- 0002-7752-01, 0002-7752-05
- Manufacturer
- Eli Lilly and Company
- Effective date
- 2025-06-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Insulin Lispro - Eli Lilly and Company | Eli Lilly and Company | 2025-06-17 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0002-7752-05 | 2024-01-30 | C162847 | 48780-1 | 1030e365-2939-111a-e063-dadaa90a10e2 | These highlights do not include all the information needed to use INSULIN LISPRO safely and effectively. See full prescribing information for INSULIN LISPRO. INSULIN LISPRO injection, for subcutaneous or intravenous use Initial U.S. Approval: 1996 This product is HUMALOG ® (insulin lispro). |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0002-7752-01 | Insulin Lispro Junior KwikPen | 3 mL in 1 SYRINGE | INJECTION, SOLUTION | 3 | 12 | |
| 0002-7752-05 | Insulin Lispro Junior KwikPen | 5 in 1 CARTON | INJECTION, SOLUTION | 5 | 12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0002-7752 | INSULIN LISPRO INJECTION, SOLUTION INSULIN LISPRO KWIKPEN (INSULIN LISPRO) INJECTION, SOLUTION INSULIN LISPRO JUNIOR KWIKPEN (INSULIN LISPRO) INJECTION, SOLUTION [ELI LILLY AND COMPANY] | 11 | Current NDC, Legacy NDC, 2 package rows | 20241213_97d5e596-aae1-42c9-ae89-c3780959c467.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0002-7752-01 | ML - Milliliter | 0002-7752 | a33dea4a-34d3-4aad-aee0-7ec8c9287ae0 | 1 | 2020-04-20 |
| 0002-7752-05 | ML - Milliliter | 0002-7752 | 4b567318-1ca3-4059-a4dc-299cfcce16c3 | 1 | 2020-04-20 |
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 |
|---|---|---|---|---|---|---|
| Walgreens Sore Throat Cherry Flavor | PHENOL | WALGREEN COMPANY | fe092017-1f3e-41f1-b718-e24de53cf276 | 2025-11-26 | Warnings | 339NCG44TV |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| Rain Daily Hydration and Comfort For Dry Eyes | GLYCERIN | Rain Eye Drops, LLC | 31d7c204-fb74-fb28-e063-6294a90ab330 | 2025-11-23 | Warnings | PDC6A3C0OX |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
| COLD/FLU HP | ARSENICTRIOXIDE,BAPTISIATINCTORIAROOT,BRYONIAALBAROOT,SOLANUMDULCAMARATOP,ECHINACEAANGUSTIFOLIA,ECHINACEAPURPUREA,EUPATORIUMPERFOLIATUMFLOWERINGTOP,FERROSOFERRICPHOSPHATE,GELSEMIUMSEMPERVIRENSROOT,POTASSIUMCHLORIDE,PHOSPHORUS,ANEMONEPULSATILLA,SULFUR,ZINCACETATEANHYDROUS,ZINCCARBONATE,ZINC,ZINCCHLORIDE,ZINCOXIDE,ZINCPICRATENONAHYRDATE,ZINCVALERATEDIHYDRATE,CAIRINAMOSCHATAHEART/LIVERAUTOLYSATE,INFLUENZINUM | Natural Creations, Inc. | 11d945ea-3b03-42cc-b1c0-e4c517e386f6 | 2025-11-20 | Warnings | J41CSQ7QDS |
| Brain Liquescence | GINKGO BILOBA, COLCHICUM AUTUMNALE, CONVALLARIA MAJALIS, NUX MOSCHATA, CEREBRUM (SUIS), AGARICUS MUSCARIUS, SCUTELLARIA LATERIFLORA, ANACARDIUM ORIENTALE, RIBOFLAVINUM, AMBRA GRISEA, BARYTA CARBONICA, GLYCERINUM | Nutritional Specialties, Inc. | a5c366f3-fd42-4602-b20b-b7b15fde564e | 2025-11-19 | Warnings | PDC6A3C0OX |
| Hemorrhoidal Cream | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Trifecta Pharmaceuticals Usa Llc | 804d7b1f-1be8-50c9-e053-2a91aa0a35d0 | 2025-11-18 | Warnings | PDC6A3C0OX |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | fd823bef-c14c-4708-a18a-8aaa8470412f | 2025-11-18 | Warnings, Adverse reactions | 059QF0KO0R |
| Antifungal cream | ANTIFUNGAL CREAM | Guangzhou Guoyoumi Biotechnology Co Ltd | 43a5b3c8-3b99-b113-e063-6394a90a9aff | 2025-11-15 | Warnings | PDC6A3C0OX |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 3765c251-eb14-d60f-e063-6294a90a6a4d | 2025-11-12 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37f244fd-c02f-e66a-e063-6394a90aed81 | 2025-11-12 | Warnings | 059QF0KO0R |
| TopCare Cherry Flavor | PHENOL | TOPCO ASSOCIATES, LLC | 5d3f0610-deb4-4180-ae19-2c65ed2f368b | 2025-11-10 | Warnings | 339NCG44TV |
| Topcare Sore Throat Menthol Flavor | PHENOL | TOPCO ASSOCIATES LLC | fb1f2c11-2508-4985-bae5-7d547bd6aa23 | 2025-11-10 | Warnings | 339NCG44TV |
| STERILE WATER | WATER | Henry Schein, Inc. | f4087143-9868-4308-b96c-43657ee8ec28 | 2025-11-07 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.