NDC 0002-3270-01 - Cymbalta
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
- 0002-3270
- Requested NDC
- 0002-3270-01
- Package NDCs from labels
- 0002-3270-30, 0002-3270-01
- Manufacturer
- Eli Lilly and Company
- Effective date
- 2025-07-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cymbalta - Eli Lilly and Company | Eli Lilly and Company | 2025-07-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Cymbalta - PD-Rx Pharmaceuticals, Inc. | PD-Rx Pharmaceuticals, Inc. | 2022-02-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Cymbalta | H.J. Harkins Company, Inc. | Eli Lilly and Company | Evonik Degussa Corporation | Lilly del Caribe, Inc. (PR06) | Lilly del Caribe, Inc. (PR01) | Eli Lilly and Company (Indianapolis) | Sharp - Conshohocken | Sharp - Allentown | 2011-10-18 | 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 |
|---|---|---|---|---|---|---|
| 0002-3270-30 | Cymbalta | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | 90 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0002-3270-01 | EA - Each | 0002-3270 | 7149c6ef-ec54-4fd3-9083-2e15125bea62 | 1 | 2012-07-24 |
| 0002-3270-04 | EA - Each | 0002-3270 | ad73f24c-7d72-4830-97ae-1a9ba1b8ec58 | 1 | 2012-07-24 |
| 0002-3270-30 | EA - Each | 0002-3270 | 581237c9-1b60-4246-8dff-bfaab7eb8898 | 1 | 2012-07-24 |
| 0002-3270-33 | EA - Each | 0002-3270 | 9366b8c5-1181-45d4-8587-e383e34e2a45 | 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 |
|---|---|---|---|---|---|---|
| MINERAL BASED SPF 50 SUNSCREEN | ZINC OXIDE, TITANIUM DIOXIDE | THE KROGER COMPANY | a4e6936d-a76c-e8fd-e053-2995a90a965f | 2024-10-15 | Warnings | 15FIX9V2JP |
| TopCare Everyday Mineral Sunscreen Continuous Broad Spectrum SPF 50 Reef-Conscious Formula | TITANIUM DIOXIDE, ZINC OXIDE | TOPCO ASSOCIATES LLC | f14f43e6-ee57-5495-e053-2a95a90a4011 | 2024-10-15 | Warnings | 15FIX9V2JP |
| MINERAL SUNSCREEN SPF 50 | ZINC OXIDE, TITANIUM DIOXIDE | TOPCO ASSOCIATES LLC | bfe076fa-f21f-2c46-e053-2a95a90acee4 | 2024-10-15 | Warnings | 15FIX9V2JP |
| H.E.B. Mineral Sunscreen Broad Spectrum SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | H.E.B. | c5279caf-3af9-d163-e053-2995a90a943b | 2024-10-15 | Warnings | 15FIX9V2JP |
| Target Up and Up Mineral Sunscreen Broad Spectrum SPF 50 Reef-Conscious Formula | TITANIUM DIOXIDE, ZINC OXIDE | TARGET CORPORATION | cfd735d2-df3a-5ed0-e053-2995a90a9f26 | 2024-10-14 | Warnings | 15FIX9V2JP |
| Target Up and Up SPF 50 Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | TARGET CORPORATION | f99028fa-a17e-4a84-e053-6294a90a927f | 2024-10-14 | Warnings | 15FIX9V2JP |
| AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.102 | ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDE | AMOREPACIFIC CORPORATION | 531f60c9-c89a-46bc-8460-d01b2e838e6f | 2024-10-08 | Warnings | 15FIX9V2JP |
| AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.104 | OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE | AMOREPACIFIC CORPORATION | 60964d9f-d96c-4397-b273-6b63d1886722 | 2024-10-08 | Warnings | 15FIX9V2JP |
| IOPE AIR CUSHION Cover 21 Vanilla | ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDE | AMOREPACIFIC CORPORATION | 29d6cc8d-1469-479d-a15a-e78d4e22d4a2 | 2024-10-08 | Warnings | 15FIX9V2JP |
| DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen | AVOBENZONE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE | PureTek Corporation | 86eb06cc-d63f-4500-a52e-14ef99a56532 | 2024-10-02 | Warnings | 15FIX9V2JP |
| Duloxetine | DULOXETINE | Proficient Rx LP | 3dec1805-9a95-462e-8784-303004d500b1 | 2024-10-01 | Boxed warning, Warnings, Adverse reactions | 596926 9044SC542W |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD | 43bec652-3f2c-4671-8a0c-c4c4a4bfcc7a | 2024-10-01 | Warnings | 15FIX9V2JP |
| Duloxetine | DULOXETINE | Camber Pharmaceuticals, Inc. | b14feecc-04c6-4b2d-ba55-2e1dbef6b0d7 | 2024-09-28 | Boxed warning, Warnings, Adverse reactions | 596926 596930 596934 9044SC542W |
| Gut Brain Spectrum | ABROTANUM (ARTEMISIA ABROTANUM), AETHUSA CYNAPIUM, BAPTISIA TINCTORIA, CICUTA VIROSA, CUPRUM METALLICUM, MEZEREUM, BUFO RANA, LAC MATERNA HUMANUM, SACCHARUM OFFICINALE, SEROTONIN (HYDROCHLORIDE), ALUMINA, CALCAREA PHOSPHORICA, CANDIDA ALBICANS, CARCINOSIN, HELIUM, LAC CANINUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, SULPHUR, THUJA OCCIDENTALIS, FORMALINUM, MORBILLINUM | Energique, Inc. | cb1566a4-92d4-4f1a-9211-f0c538a83c27 | 2024-09-27 | Warnings | C151H8M554 |
| Household Antigens | ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR | Energique, Inc. | 87c92497-8a51-4977-87fe-e0b4c6bafb19 | 2024-09-27 | Warnings | 368GB5141J |
| Advanced Eye Relief/ Redness Maximum Relief | NAPHAZOLINE HYDROCHLORIDE AND HYPROMELLOSE | Bausch & Lomb Incorporated | 3c11285a-7e86-4b47-b1ee-e7d59858087d | 2024-09-25 | Warnings | 3NXW29V3WO |
| PMS Relief | AGNUS CASTUS, AURUM SULPHURATUM, CANDIDA ALBICANS, CIMICIFUGA RACEMOSA, COCCULUS INDICUS, CONIUM MACULATUM, CYCLAMEN EUROPAEUM, ELAPS CORALLINUS, FOLLICULINUM, HYPOTHALAMUS SUIS, KALI CARBONICUM, LAC CANINUM, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, MAGNESIA CARBONICA, PULSATILLA (PRATENSIS), SACCHARUM OFFICINALE, STANNUM METALLICUM, THUJA OCCIDENTALIS, THYROIDINUM (BOVINE) | Deseret Biologicals, Inc. | f03d8463-0a6d-4577-8fba-9cba246d3d45 | 2024-09-23 | Warnings | C151H8M554 |
| Focus | GINKGO BILOBA, ALPHA-KETOGLUTARICUM ACIDUM, IODIUM, PHOSPHORUS, SARCOLACTICUM ACID, SACCHARUM OFFICINALE, ADENOSINUM CYCLOPHOSPHORICUM, CEREBRUM SUIS, HYPOTHALAMUS SUIS, SILICEA, ADRENALINUM, AMBRA GRISEA, CARBONEUM SULPHURATUM, TARENTULA HISPANA, AETHUSA CYNAPIUM, BARYTA CARBONICA, HELLEBORUS NIGER, VERATRUM ALBUM, CANDIDA ALBICANS, HYOSCYAMUS NIGER | Deseret Biologicals, Inc. | e77857b8-be67-4041-8c8d-9772f17c6d06 | 2024-09-11 | Warnings | C151H8M554 |
| PMS Relief | AGNUS CASTUS, CIMICIFUGA RACEMOSA, KALI CARBONICUM, LYCOPODIUM CLAVATUM, SACCHARUM OFFICINALE, THYROIDINUM (BOVINE), HYPOTHALAMUS SUIS, ARISTOLOCHIA CLEMATITIS, FOLLICULINUM, AURUM SULPHURATUM, CANDIDA ALBICANS, COCCULUS INDICUS, CONIUM MACULATUM, CYCLAMEN EUROPAEUM, ELAPS CORALLINUS, LAC CANINUM, LACHESIS MUTUS, MAGNESIA CARBONICA, PULSATILLA (PRATENSIS), STANNUM METALLICUM | Deseret Biologicals, Inc. | ca073beb-330d-406c-9bf5-196a89f3ab58 | 2024-09-11 | Warnings | C151H8M554 |
| Proceuticals Private Label by TiZO tinted mineral sunscreen stick | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, Ltd | 2179a2ff-9425-5b2c-e063-6294a90a45b6 | 2024-09-06 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.