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 |
|---|---|---|---|---|---|---|
| Duloxetine | DULOXETINE | REMEDYREPACK INC. | c66fb2ee-f64a-4d28-a692-e8dc7b61fbc9 | 2026-07-14 | Boxed warning, Warnings, Adverse reactions | 596926 9044SC542W |
| Duloxetine | DULOXETINE | ANI Pharmaceuticals, Inc. | fb37745f-fb40-4f7f-8143-ea1874c38e1b | 2026-07-13 | Boxed warning, Warnings, Adverse reactions | 596926 596930 596934 9044SC542W |
| Duloxetine | DULOXETINE | REMEDYREPACK INC. | 1d3a45f3-3854-4d0c-9241-770aa24063fd | 2026-07-10 | Boxed warning, Warnings, Adverse reactions | 596930 9044SC542W |
| Bombee Honey Daily Glow Shield Sunscreen | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE | ABT ASIA Inc. | 56112dff-b091-7a56-e063-6294a90a77d3 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | DERMIO DERMATOLOGY LLC | 562f5b0d-6a10-305d-e063-6394a90a5980 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Suzanne's Skin2soul LLC | 562fbaa6-f93a-5ec4-e063-6294a90a9634 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Aussie Betta Tallow Sunscreen SPF50 SPF50 | TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN | AUSSIE BETTA HEALTHY CARE PTY LTD | 56007d82-ff5b-6c26-e063-6294a90a09b6 | 2026-07-07 | Warnings | 15FIX9V2JP |
| Artificial Tears | ARTIFICIAL TEARS | AvPAK | f18bebf2-1936-658f-e053-2a95a90a5012 | 2026-07-07 | Warnings | 3NXW29V3WO |
| EELHOE Body Coverage Perfector | TITANIUM DIOXIDE | Shantou Eelhoe Daily Chemical Technology Co., Ltd. | 5610c3b7-456b-3bc1-e063-6394a90a3fa8 | 2026-07-07 | Warnings | 15FIX9V2JP |
| DULOXETINE HYDROCHLORIDE | DULOXETINE HYDROCHLORIDE | Yaopharma Co., Ltd. | 90224073-178d-7ec5-e053-2995a90a20fc | 2026-07-07 | Boxed warning, Warnings, Adverse reactions | 596926 596930 596934 9044SC542W |
| Premier Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Emerald Aesthetics LLC | 55f88dd1-346c-22a5-e063-6294a90a711f | 2026-07-06 | Warnings | 15FIX9V2JP |
| Duloxetine | DULOXETINE | REMEDYREPACK INC. | b149641a-03e6-4fee-91f3-7ba8e01196bd | 2026-07-02 | Boxed warning, Warnings, Adverse reactions | 596930 9044SC542W |
| OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige | TITANIUM DIOXIDE | LG H&H Co., Ltd. | d307471c-6cc6-ce48-e053-2995a90a3e02 | 2026-07-02 | Warnings | 15FIX9V2JP |
| Evereden Fluid Silk Mineral Sunscreen PRO SPF50 | TITANIUM DIOXIDE, ZINC OXIDE | Eden Brands Inc. | 2cb7773f-9a05-ad02-e063-6294a90af024 | 2026-07-01 | Warnings | 15FIX9V2JP |
| OHUI Ultimate Cover CC Cushion Compact 01 Light Beige | TITANIUM DIOXIDE | LG H&H Co., Ltd. | d2f9c54b-ac4e-5141-e053-2a95a90aa2b8 | 2026-06-30 | Warnings | 15FIX9V2JP |
| Duloxetine | DULOXETINE | St. Mary's Medical Park Pharmacy | 39fa4247-e864-f653-e063-6394a90ac98d | 2026-06-30 | Boxed warning, Warnings, Adverse reactions | 596926 9044SC542W |
| TOCOBO Blur Finish Sun Cushion Cotton Blue | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | PICTON Co., Ltd. | 4d6ddee3-9a76-6c9c-e063-6394a90a1529 | 2026-06-29 | Warnings | 15FIX9V2JP |
| Earth Baby Broad Spectrum SPF 30 | SUNSCREEN | Earth Baby, Inc. | 42556876-74ea-38e6-e054-00144ff8d46c | 2026-06-28 | Warnings | 15FIX9V2JP |
| Sun Does Matter Daily Face Sunscreen | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE | Sundoesmatter Company Inc. | 553687d8-d4e1-8361-e063-6294a90a24fe | 2026-06-27 | Warnings | 15FIX9V2JP |
| Ivory Perfecting Makeup Broad Spectrum SPF 25 | OCTINOXATE, TITANIUM DIOXIDE | Merle Norman Cosmetics, Inc | 552f25ba-61d5-6a94-e063-6394a90a46e9 | 2026-06-26 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.