Home NDC 70518-3829-01 NDC 70518-3829-01 - FAMOTIDINE 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 70518-3829
Requested NDC 70518-3829-01
Package NDCs from labels 70518-3829-0, 70518-3829-1, 70518-3829-2, 70518-3829-3, 70518-3829-4, 70518-3829-5, 70518-3829-6, 70518-3829-7, 70518-3829-8, 70518-3829-9, 70518-3829-01
Manufacturer REMEDYREPACK INC.
Effective date 2026-06-09
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type FAMOTIDINE - REMEDYREPACK INC. REMEDYREPACK INC. 2026-06-09 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-3829-0 FAMOTIDINE 50 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 50 13 70518-3829-1 FAMOTIDINE 30 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 30 13 70518-3829-2 FAMOTIDINE 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 13 70518-3829-3 FAMOTIDINE 90 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 90 13 70518-3829-4 FAMOTIDINE 90 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 90 13 70518-3829-5 FAMOTIDINE 30 in 1 BLISTER PACK TABLET, FILM COATED 30 13 70518-3829-6 FAMOTIDINE 14 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 14 13 70518-3829-7 FAMOTIDINE 60 in 1 BLISTER PACK TABLET, FILM COATED 60 13 70518-3829-8 FAMOTIDINE 14 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 14 13 70518-3829-9 FAMOTIDINE 25 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 25 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-3829 FAMOTIDINE TABLET, FILM COATED [REMEDYREPACK INC.] 10 Current NDC, 10 package rows 20250115_e59a2c97-19c7-485c-bb1b-272ddb9ae053.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 59 of 119 · 2,375 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join MOOYAM Dark Skin Sunscreen SUNSCREEN Guangdong Bisutang Biotechnology Co., LTD 4246e9f1-1c51-d888-e063-6394a90abda0 2025-10-29 Warnings Exact identifier unii: 15FIX9V2JP non-tinted mineral sunscreen TITANIUM DIOXIDE, ZINC OXIDE Clove Hill LLC 311b270f-b9e2-2374-e063-6294a90af581 2025-10-29 Warnings Exact identifier unii: 15FIX9V2JP Perricone MD Neuropeptide Restorative Neck and Chest Therapy Broad Spectrum SPF 25 TITANIUM DIOXIDE THG Beauty USA LLC 23f4cf41-0eed-2df3-e063-6294a90ad402 2025-10-28 Warnings Exact identifier unii: 15FIX9V2JP PERRICONE MD VITAMIN C ESTER PHOTO-BRIGHTENING MOISTURIZER BROAD SPECTRUM SPF 30 TITANIUM DIOXIDE THG Beauty USA LLC 397b4338-fec8-5228-e063-6394a90ad97d 2025-10-23 Warnings Exact identifier unii: 15FIX9V2JP Perricone MD HIGH POTENCY CLASSICS Face Finishing and Firming Tinted Moisturizer Broad Spectrum SPF 30 TITANIUM DIOXIDE THG Beauty USA LLC 38c80373-1d5a-c7f4-e063-6294a90aa9c2 2025-10-23 Warnings Exact identifier unii: 15FIX9V2JP Perricone MD Cold Plasma Plus Daily Defense Moisturizer Broad Spectrum SPF 35 ZINC OXIDE, TITANIUM DIOXIDE THG Beauty USA LLC 254b4692-a459-6119-e063-6394a90a0a60 2025-10-23 Warnings Exact identifier unii: 15FIX9V2JP FAMOTIDINE FAMOTIDINE Bryant Ranch Prepack 7cef62ab-1740-4d0f-b6ea-fda783e1c197 2025-10-23 Warnings, Adverse reactions Exact identifier application number: ANDA215630 rxcui: 284245 unii: 5QZO15J2Z8 No7 Lift and Luminate Triple Action Serum Foundation Sunscreen Broad Spectrum SPF 15 Latte OCTINOXATE, TITANIUM DIOXIDE BCM Cosmetique SAS c34c1486-fa6c-485f-80b3-98e397b3dddb 2025-10-22 Warnings Exact identifier unii: 15FIX9V2JP No7 Lift and Luminate Triple Action Serum Foundation Sunscreen Broad Spectrum SPF 15 Cool Vanilla OCTINOXATE, TITANIUM DIOXIDE BCM Cosmetique SAS 74c078ec-a371-4406-8d5e-a0baada3a1a6 2025-10-22 Warnings Exact identifier unii: 15FIX9V2JP No7 Lift and Luminate Triple Action Serum Foundation Sunscreen Broad Spectrum SPF 15 Sandalwood OCTINOXATE, TITANIUM DIOXIDE BCM Cosmetique SAS 2765f345-eab2-4878-b1f1-f8e243083476 2025-10-22 Warnings Exact identifier unii: 15FIX9V2JP No7 Lift and Luminate Triple Action Serum Foundation Sunscreen Broad Spectrum SPF 15 Toffee OCTINOXATE, TITANIUM DIOXIDE BCM Cosmetique SAS d1181543-07ab-4a51-8b55-afc1a98293f6 2025-10-22 Warnings Exact identifier unii: 15FIX9V2JP No7 Lift and Luminate Triple Action Serum Foundation Sunscreen Broad Spectrum SPF 15 Warm Beige OCTINOXATE, TITANIUM DIOXIDE BCM Cosmetique SAS c7be3a7e-f031-4ec0-b9dc-41c025cd0066 2025-10-22 Warnings Exact identifier unii: 15FIX9V2JP Powder TITANIUM DIOXIDE Oxygen Development LLC 41c0c262-21c3-b8e6-e063-6394a90a7c9c 2025-10-22 Warnings Exact identifier unii: 15FIX9V2JP Famotidine FAMOTIDINE PD-Rx Pharmaceuticals, Inc. 002875d2-8c30-2d2e-e063-6294a90ae01e 2025-10-22 Warnings, Adverse reactions Exact identifier rxcui: 310273 unii: 5QZO15J2Z8 Sonni SunDay Invisible Defense TITANIUM DIOXIDE, ZINC OXIDE Sonni 41ad9658-7906-d04c-e063-6394a90a4723 2025-10-21 Warnings Exact identifier unii: 15FIX9V2JP Sonni SunDay Body Balm TITANIUM DIOXIDE, ZINC OXIDE Sonni 41adca2e-cf69-ccd9-e063-6294a90a0dc0 2025-10-21 Warnings Exact identifier unii: 15FIX9V2JP e l f Camo Semi Matte CC SPF 30 Deep 530 W ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE e.l.f. Cosmetics, Inc. 940e0b2d-0b10-4534-ba36-e9980cead492 2025-10-21 Warnings Exact identifier unii: 15FIX9V2JP Clinical Skin Filter Tinted Sunscreen CLINICAL SKIN FILTER TINTED SUNSCREEN KRX RESOURCES SDN. BHD. 22b8856b-671f-def3-e063-6394a90a4ea0 2025-10-18 Warnings Exact identifier unii: 15FIX9V2JP Clinical Skin Filter Tinted Sunscreen Medium Dark CLINICAL SKIN FILTER TINTED SUNSCREEN MEDIUM DARK KRX RESOURCES SDN. BHD. 22cead37-f862-e859-e063-6394a90a86ce 2025-10-18 Warnings Exact identifier unii: 15FIX9V2JP Krx Aesthetics All Day Glow Sunblocker KRX AESTHETICS ALL DAY GLOW SUNBLOCKER KRX RESOURCES SDN. BHD. 22a60fb9-0fea-92c0-e063-6394a90a088c 2025-10-18 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.