NDC 0002-4454-01 - Zyprexa
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
- 0002-4454
- Requested NDC
- 0002-4454-01
- Package NDCs from labels
- 0002-4454-01, 0002-4454-85
- Manufacturer
- Eli Lilly and Company
- Effective date
- 2025-11-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Zyprexa - Eli Lilly and Company | Eli Lilly and Company | 2025-11-18 | 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0002-4454-01 | ZYPREXA Zydis | 1 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 1 | 67 | |
| 0002-4454-01 | ZYPREXA Zydis | 1 in 1 DOSE PACK | TABLET, ORALLY DISINTEGRATING | 1 | 67 | |
| 0002-4454-85 | ZYPREXA Zydis | 30 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 30 | 67 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0002-4454 | ZYPREXA (OLANZAPINE) TABLET ZYPREXA ZYDIS (OLANZAPINE) TABLET, ORALLY DISINTEGRATING ZYPREXA INTRAMUSCULAR (OLANZAPINE) INJECTION, POWDER, FOR SOLUTION [ELI LILLY AND COMPANY ] | 66 | Legacy NDC, 3 package rows | 20250110_d5051fbc-846b-4946-82df-341fb1216341.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0002-4454-01 | EA - Each | 0002-4454 | 7e221558-7584-4b8b-b359-bbce11fe7e20 | 1 | 2012-07-24 |
| 0002-4454-85 | EA - Each | 0002-4454 | 9879037d-1deb-4639-8596-ead22339987d | 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 |
|---|---|---|---|---|---|---|
| Cetaphil Redness Relieving Daily Facial Moisturizer with sunscreen SPF 40 | TITANIUM DIOXIDE, ZINC OXIDE | Galderma Laboratories, L.P. | 45d101be-2b88-4759-9ccc-556f5ec0553d | 2025-12-17 | Warnings | 15FIX9V2JP |
| Brightening Primer SPF 20 | TITANIUM DIOXIDE AND ZINC OXIDE | Colorescience | a42d6761-47cd-4c9b-9656-64e37e065639 | 2025-12-17 | Warnings | 15FIX9V2JP |
| Bronzing Primer SPF 20 | TITANIUM DIOXIDE AND ZINC OXIDE | Colorescience | f749af07-0fcd-4376-be62-7c078b3e7eb6 | 2025-12-17 | Warnings | 15FIX9V2JP |
| SUNSCREEN Stick | ZINC OXIDE 15%, TITANIUM DIOXIDE 8%, HOMOSALATE 6% | Foshan Sugar Max Cosmetics CO.,Ltd | 460e1038-30f0-a6e4-e063-6394a90ad534 | 2025-12-16 | Warnings | 15FIX9V2JP |
| SUNSCREEN SPRAY150ml | ZINC OXIDE 15%, TITANIUM DIOXIDE 6%, HOMOSALATE 5%, OCTISALATE 4% | Foshan Sugar Max Cosmetics CO.,Ltd | 460ead6c-dd44-e320-e063-6294a90a2b64 | 2025-12-16 | Warnings | 15FIX9V2JP |
| Sunscreen Cream | ZINC OXIDE 12%,TITANIUM DIOXIDE 8%, HOMOSALATE 12%, OCTISALATE4.5%,PHENYLBENZIMIDAZOLE SULFONIC ACID 3.5% | Foshan Sugar Max Cosmetics CO.,Ltd | 460f0ca0-9440-9a6e-e063-6394a90a33b3 | 2025-12-16 | Warnings | 15FIX9V2JP |
| Non Tinted Facial Mineral Protectant | TITANIUM DIOXIDE, ZINC OXIDE | EUROPEAN SKIN AND MASSAGE STUDIO | 3766496f-231c-f98c-e063-6294a90aae08 | 2025-12-16 | 15FIX9V2JP | |
| Tinted Facial Mineral Protectant | TITANIUM DIOXIDE, ZINC OXIDE | EUROPEAN SKIN AND MASSAGE STUDIO | 3766b0d8-20e6-a227-e063-6294a90af4da | 2025-12-16 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen Broad Spectrum SPF 40 | TITANIUM DIOXIDE, ZINC OXIDE | WECARE FRISCO PLLC | 374f866d-eb52-61e3-e063-6394a90a77c7 | 2025-12-16 | 15FIX9V2JP | |
| Tinted Lip Protection | TITANIUM DIOXIDE, ZINC OXIDE | WECARE FRISCO PLLC | 3750c23d-c3f8-fac3-e063-6394a90a135e | 2025-12-16 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | KATHY JONES AESTHETHICS LLC | 37dab729-5988-5eba-e063-6294a90ac6b7 | 2025-12-16 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Tory Sullivan, M.D., P.A. | 36241e60-f02a-50a7-e063-6394a90a6390 | 2025-12-16 | 15FIX9V2JP | |
| UV Defense Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | CCLEAR SOLUTIONS ACNE & SKIN CARE CLINIC | 365e09a8-308b-b753-e063-6394a90ae9e5 | 2025-12-16 | 15FIX9V2JP | |
| UV Defense Mineral Sunscreen Tinted | TITANIUM DIOXIDE, ZINC OXIDE | CCLEAR SOLUTIONS ACNE & SKIN CARE CLINIC | 365e2498-7df2-f22c-e063-6294a90ac6ab | 2025-12-16 | 15FIX9V2JP | |
| UV Protection Veil Mineral Sunscreen non tinted | TITANIUM DIOXIDE, ZINC OXIDE | ATHENA PLASTIC SURGERY | 3b3bf5a6-33ec-0255-e063-6294a90ac96a | 2025-12-16 | Warnings | 15FIX9V2JP |
| UV Protection Veil Mineral Sunscreen, tinted | TITANIUM DIOXIDE, ZINC OXIDE | ATHENA PLASTIC SURGERY | 3b3cba2e-acc6-a2df-e063-6294a90abf71 | 2025-12-16 | Warnings | 15FIX9V2JP |
| UV Protection Veil Mineral Sunscreen, tinted | TITANIUM DIOXIDE, ZINC OXIDE | ATHENA PLASTIC SURGERY | 3b3c757f-6581-4978-e063-6294a90a6173 | 2025-12-16 | Warnings | 15FIX9V2JP |
| Virgo SOL Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ULTRAVIOLET SKINCARE LLC | 369d4f43-8c57-9fcf-e063-6294a90aa916 | 2025-12-16 | 15FIX9V2JP | |
| Virgo SOL Non Tinted Mousse | TITANIUM DIOXIDE, ZINC OXIDE | ULTRAVIOLET SKINCARE LLC | 369d63a9-b9ab-9530-e063-6394a90ac8ef | 2025-12-16 | 15FIX9V2JP | |
| Kind Restore Moisturizing Lip Balm | TITANIUM DIOXIDE, ZINC OXIDE | POLISH BEAUTY | 39814e27-4f3f-5ee6-e063-6394a90a941b | 2025-12-16 | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.