Home NDC 70518-1244-01 NDC 70518-1244-01 - Duloxetine 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 70518-1244
Requested NDC 70518-1244-01
Package NDCs from labels 70518-1244-0, 70518-1244-1, 70518-1244-2, 70518-1244-3, 70518-1244-5, 70518-1244-4, 70518-1244-7, 70518-1244-6, 70518-1244-8, 70518-1244-9, 70518-1244-01
Manufacturer REMEDYREPACK INC.
Effective date 2026-08-10
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Duloxetine - REMEDYREPACK INC. REMEDYREPACK INC. 2026-08-10 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-1244-0 Duloxetine 30 in 1 BLISTER PACK CAPSULE, DELAYED RELEASE 30 14 70518-1244-1 Duloxetine 60 in 1 BOTTLE, PLASTIC CAPSULE, DELAYED RELEASE 60 14 70518-1244-2 Duloxetine 180 in 1 BOTTLE, PLASTIC CAPSULE, DELAYED RELEASE 180 14 70518-1244-3 Duloxetine 30 in 1 BLISTER PACK CAPSULE, DELAYED RELEASE 30 14 70518-1244-4 Duloxetine 50 in 1 BOX CAPSULE, DELAYED RELEASE 50 14 70518-1244-5 Duloxetine 1 in 1 POUCH CAPSULE, DELAYED RELEASE 1 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-1244 DULOXETINE CAPSULE, DELAYED RELEASE [REMEDYREPACK INC.] 8 Current NDC, Legacy NDC, 6 package rows 20250509_461d769c-b787-4bc7-b4a6-7a5f33ae9d45.zip
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.
Matched openFDA labels page 65 of 114 · 2,267 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Systane Ultra POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL Alcon Laboratories, Inc. 0537c23a-15f7-be64-1231-a6c93468e9a8 2025-07-30 Warnings Exact identifier unii: 6DC9Q167V3 Systane POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL Alcon Laboratories, Inc. 1d679d0f-cec2-a644-79cd-079607254bb9 2025-07-30 Warnings Exact identifier unii: 6DC9Q167V3 Systane Ultra Preservative Free POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL Alcon Laboratories, Inc. 751fb85f-6683-4b0a-a650-324d4a74c5de 2025-07-30 Warnings Exact identifier unii: 6DC9Q167V3 Systane COMPLETE PF PROPYLENE GLYCOL Alcon Laboratories, Inc. 99b63d62-1cf0-4f28-8760-773917c2538a 2025-07-29 Warnings Exact identifier unii: 6DC9Q167V3 Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Kenvue Brands LLC 003123d2-9675-fdd2-e063-6294a90a0130 2025-07-28 Warnings Exact identifier unii: 15FIX9V2JP Neutrogena Mineral Ultra Sheer Face SPF 70 TITANIUM DIOXIDE, ZINC OXIDE Kenvue Brands LLC 20e0badf-fe25-1d27-e063-6294a90a7cfe 2025-07-28 Warnings Exact identifier unii: 15FIX9V2JP Duloxetine D/R DULOXETINE D/R Direct_Rx 3ac53025-8a99-31de-e063-6294a90a53d2 2025-07-25 Boxed warning, Warnings, Adverse reactions Exact identifier application number: ANDA090694 rxcui: 596926 unii: 9044SC542W Dolce and Gabbana Everlast Foundation SPF 20 01N Light OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE Dolce & Gabbana Beauty S.R.L 2ccf4e45-4cec-417d-9f4c-28f376025f1d 2025-07-25 Warnings Exact identifier unii: 15FIX9V2JP Sunscreen TITANIUM DIOXIDE 6.8% Baxter of California, LLC 146030bc-2bf4-25ea-e063-6294a90a4613 2025-07-24 Warnings Exact identifier unii: 15FIX9V2JP La Defense Broad Spectrum SPF 30 Mineral Sunscreen ZINC OXIDE, TITANIUM DIOXIDE Luzern Laboratories, Inc 3f00befa-415d-415d-89e1-6ba8770ba51e 2025-07-21 Warnings Exact identifier unii: 15FIX9V2JP Smelling Salts SMELLING SALTS Shenzhen Weikeduo E-commerce Co., Ltd. 377fa82a-dcbe-9ab6-e063-6394a90a6384 2025-07-18 Warnings Exact identifier unii: 5138Q19F1X Amarte ULTRA VEIL Daily SUNSCREEN Amarte USA LLC 39e9ca98-d0e8-6b8f-e063-6394a90aa366 2025-07-15 Warnings Exact identifier unii: 15FIX9V2JP Amarte ULTRA VEIL BB Fair SUNSCREEN Amarte USA LLC 39e87950-4103-c2eb-e063-6394a90a0552 2025-07-15 Warnings Exact identifier unii: 15FIX9V2JP Gluvelop SMELLING SALTS SMELLING SALTS Shenzhen Nanjun Technology Co., Ltd 398c26ec-5eba-1202-e063-6294a90a76c9 2025-07-09 Warnings Exact identifier unii: 5138Q19F1X Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE CAPE COD SKIN CARE CO. INC. 39093b2d-3fbb-8378-e063-6294a90ac6d8 2025-07-03 Exact identifier unii: 15FIX9V2JP Vertra S Dorian Kona Gold Signature Face Stick SPF 38 TITANIUM DIOXIDE Toshiki Pigment Co., ltd. b7162a2f-07f1-6188-e053-2995a90a8a9c 2025-06-27 Warnings Exact identifier unii: 15FIX9V2JP Steritalc 2g TALC Novatech SA c94e51d9-beef-4b06-e053-2a95a90a754a 2025-06-25 Warnings, Adverse reactions Exact identifier unii: 7SEV7J4R1U MELAO WHITENING SUNSCREEN TITANIUM DIOXIDE Guangdong Aimu Biological Technology Co., Ltd 1aaf5942-ff13-ee07-e063-6394a90acd28 2025-06-25 Warnings Exact identifier unii: 15FIX9V2JP BISUTANG Sunscreen BISUTANG SUNSCREEN Guangdong Bisutang Biotechnology Co Ltd 37fdb01b-929e-6a60-e063-6394a90a94e0 2025-06-20 Exact identifier unii: 15FIX9V2JP Double Use Compact SPF 15 gold deluxe edition Claire 1-2-3 OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE Bel Star S.A. (Colombia) b3747373-ef67-89ff-e053-2995a90afcde 2025-06-20 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.