NDC 62034-021-11 - DULOXETINE DELAYED-RELEASE
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
- 62034-021
- Requested NDC
- 62034-021-11
- Package NDCs from labels
- 62034-021-11, 62034-021-77
- Manufacturer
- Blenheim Pharmacal, Inc.
- Effective date
- 2016-06-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DULOXETINE DELAYED-RELEASE - Blenheim Pharmacal, Inc. | Blenheim Pharmacal, Inc. | 2016-06-07 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62034-021-77 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-1c92-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use Duloxetine Delayed-release Capsules safely and effectively. See full prescribing information for Duloxetine Delayed-release Capsules. DULOXETINE delayed-release capsules USP for oral use. Initial U.S. Approval: 2004 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62034-021-11 | DULOXETINEDELAYED-RELEASE | 1 in 1 BLISTER PACK | CAPSULE, DELAYED RELEASE PELLETS | 1 | 4 | |
| 62034-021-77 | DULOXETINEDELAYED-RELEASE | 100 in 1 BOX, UNIT-DOSE | CAPSULE, DELAYED RELEASE PELLETS | 100 | 4 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20 Cameo Glow | YOUR NAME MINERAL SHEER TINT | PML NYC, LLC | 316cd602-8af5-fbb6-e063-6294a90a287b | 2026-04-15 | Warnings | 15FIX9V2JP |
| BANANA BOAT | TITANIUM DIOXIDE,ZINC OXIDE | Edgewell Personal Care Brands LLC | 4f5896a6-0639-5589-e063-6294a90a45a9 | 2026-04-13 | Warnings | 15FIX9V2JP |
| Artificial Tears Lubricant Eye Drops | GLYCERIN, PROPYLENE GLYCOL | CVS Pharmacy | 28297fee-8185-4869-8f39-5bfbf8bf8bfd | 2026-04-13 | Warnings | 6DC9Q167V3 |
| Retaine Ultra PF | POLYETHYLENE GLYCOL | OCuSOFT LLC | a5aaaf06-772d-44d3-8601-f978ddc48ad7 | 2026-04-13 | Warnings | 6DC9Q167V3 |
| TRUST MD SPF30 STEM CELL FACE | OCTINOXATE OCTISALATE HOMOSALATE AVOBENZONE TITANIUM DIOXIDE | Guangzhou Yapheon Health Industry Co., Ltd. | 4f2ca12c-bc6f-61b8-e063-6294a90a0d7e | 2026-04-11 | Warnings | 15FIX9V2JP |
| Exovisse Preservative-Free Artificial Tears | LUBRICANT EYE GEL DROPS | YD BIO USA, INC. | 4f20191a-9124-2525-e063-6294a90a8428 | 2026-04-10 | Warnings | 3NXW29V3WO |
| Duloxetine | DULOXETINE | QPharma, Inc. | 4f205401-39ac-7009-e063-6394a90aaa8c | 2026-04-10 | Boxed warning, Warnings, Adverse reactions | 596934 9044SC542W |
| Connection | ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA, GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS | Deseret Biologicals, Inc. | 4a8be3aa-9bd9-4bb1-af98-a940c13b2bd0 | 2026-04-10 | Warnings | C151H8M554 |
| Connection | ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA, GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS | Deseret Biologicals, Inc. | 214eb19a-e7a2-421c-9f34-724ce430185c | 2026-04-10 | Warnings | C151H8M554 |
| uLOOK Sunscreen SPF 50 | SUNSCREEN | HAMEX GLOBAL COSMETICS LLC | 4e05588c-486b-60e0-e063-6294a90af457 | 2026-04-09 | Warnings | 15FIX9V2JP |
| Duloxetine | DULOXETINE | Preferred Pharmaceuticals Inc. | 9141b9d3-8d4d-43ec-acf9-e1b620590c4b | 2026-04-09 | Boxed warning, Warnings, Adverse reactions | 596930 9044SC542W |
| Duloxetine | DULOXETINE | Preferred Pharmaceuticals Inc. | e86eb765-ac9c-4ed9-bce8-819151559394 | 2026-04-08 | Boxed warning, Warnings, Adverse reactions | 596930 9044SC542W |
| Neutrogena MINERAL UV TINT FACE DEEP SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef430e8-cdc8-2897-e063-6394a90a3ac7 | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena MINERAL UV TINT FACE LIGHT SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef4a822-a7ab-b374-e063-6394a90a8508 | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena MINERAL UV TINT FACE MEDIUM SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef4d44e-3421-535f-e063-6294a90a2fea | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30 and Neutrogena Collagen Bank Moisturizer | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Acupac Packaging, Inc. | 4ef5baf7-00b1-97aa-e063-6294a90aab9c | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Ultra Sheer Face SPF 70 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef5dcd4-b2d0-bcd1-e063-6294a90a871f | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef6b5fb-5495-001c-e063-6394a90ab7b3 | 2026-04-08 | Warnings | 15FIX9V2JP |
| Duloxetine Delayed-Release | DULOXETINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 29eacc40-cbec-4cc9-8556-773346617e85 | 2026-04-08 | Boxed warning, Warnings, Adverse reactions | ANDA203088 596926 9044SC542W |
| Nu Colour Bioadaptive BB Plus Foundation - Light Golden | TITANIUM DIOXIDE | NSE Products, Inc. | faae6f47-19f3-41cb-8e0d-388569b5c73d | 2026-04-07 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.