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 60 of 119 · 2,375 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Famotidine FAMOTIDINE PD-Rx Pharmaceuticals, Inc. 66f0bf15-ff35-426a-b40c-0d0da79d0861 2025-10-16 Warnings, Adverse reactions Exact identifier rxcui: 310273 unii: 5QZO15J2Z8 Famotidine FAMOTIDINE PD-Rx Pharmaceuticals, Inc. 09ef39a4-c6b3-4395-8211-3f551dc44830 2025-10-16 Warnings, Adverse reactions Exact identifier rxcui: 284245 unii: 5QZO15J2Z8 DD Cream DD CREAM DERMAdoctor, Inc. 08c9a0cf-ee78-483b-e054-00144ff88e88 2025-10-16 Warnings Exact identifier unii: 15FIX9V2JP IBUPROFEN AND FAMOTIDINE IBUPROFEN AND FAMOTIDINE PHOENIX RX LLC 3ff33400-30e8-87fa-e063-6394a90a7f5c 2025-10-15 Boxed warning, Warnings, Adverse reactions Exact identifier unii: 5QZO15J2Z8 Ciele Filter and Protect TITANIUM DIOXIDE, ZINC OXIDE Ciele 0309b0ef-baca-b41d-e063-6294a90a49d7 2025-10-15 Warnings Exact identifier unii: 15FIX9V2JP Defend and Balance TInted Mineral Sunscreen SPF 50 SUNSCREEN Epicuren Discovery 41367f05-59d8-6736-e063-6394a90a5f17 2025-10-15 Warnings Exact identifier unii: 15FIX9V2JP Famotidine FAMOTIDINE PD-Rx Pharmaceuticals, Inc. 5798d282-ce83-49aa-bc33-13203f2b5285 2025-10-15 Warnings, Adverse reactions Exact identifier rxcui: 284245 unii: 5QZO15J2Z8 acid reducer complete FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE Safeway 4f0a178c-d0ed-4bbc-a8ce-fda3789d25f0 2025-10-14 Warnings Exact identifier unii: 5QZO15J2Z8 Famotidine FAMOTIDINE PD-Rx Pharmaceuticals, Inc. 2f5ec69d-926c-47a2-be47-8fef2e0ff207 2025-10-14 Warnings, Adverse reactions Exact identifier rxcui: 284245 unii: 5QZO15J2Z8 Famotidine FAMOTIDINE Bryant Ranch Prepack c133a9e1-ca48-4ee2-8768-01f44f5dd511 2025-10-14 Warnings, Adverse reactions Exact identifier rxcui: 310273 unii: 5QZO15J2Z8 Skinlycious Multi Protection Mineral Sunscreen Broad Spectrum SPF 30 TITANIUM DIOXIDE , ZINC OXIDE Skinlycious Pte Ltd e0ad02c3-f5ed-4b72-ba96-07d9c489a4ea 2025-10-13 Warnings Exact identifier unii: 15FIX9V2JP FAMOTIDINE FAMOTIDINE A-S Medication Solutions 3c32f8e2-f54a-422d-9c25-68692ea09001 2025-10-10 Warnings, Adverse reactions Exact identifier application number: ANDA215630 rxcui: 310273 unii: 5QZO15J2Z8 Vertra S Dorian Kona Gold Signature Face Stick SPF 38 TITANIUM DIOXIDE Eai-jr 286, Inc b6c316c3-661b-6428-e053-2a95a90a1a6b 2025-10-10 Warnings Exact identifier unii: 15FIX9V2JP FAMOTIDINE FAMOTIDINE PD-Rx Pharmaceuticals, Inc. a3b50576-cd40-4f7e-9506-bd0a61988424 2025-10-09 Warnings, Adverse reactions Exact identifier application number: ANDA215630 rxcui: 284245 unii: 5QZO15J2Z8 Dr Lift Mineral SPF 50 TITANIUM DIOXIDE, ZINC OXIDE Spa de Soleil 40c03d65-8d09-371a-e063-6294a90a7ac6 2025-10-09 Warnings Exact identifier unii: 15FIX9V2JP Dr Lift Mineral SPF 30 TITANIUM DIOXIDE Spa de Soleil 40c0e0d2-2c1d-e629-e063-6394a90a5aaf 2025-10-09 Warnings Exact identifier unii: 15FIX9V2JP Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Allergan, Inc. 29817fdc-f14c-4013-a8ed-4367f3b2867c 2025-10-09 Warnings Exact identifier unii: 15FIX9V2JP Vertra Pearl White Face Stick SPF 50 PADIMATE O, TITANIUM DIOXIDE Eai-jr 286, Inc b69a75e0-8724-35ae-e053-2a95a90a5f34 2025-10-07 Warnings Exact identifier unii: 15FIX9V2JP Vertra Mick Fanning Signature Foundation Sunscreen Face Stick SPF 35 Coolangatta Beige TITANIUM DIOXIDE EAI-JR 286, Inc. b9ea12e8-6ed9-d805-e053-2a95a90aa107 2025-10-07 Warnings Exact identifier unii: 15FIX9V2JP SPF50 Sunscreen SUNSCREEN KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD b3cde609-7d62-2ac7-e053-2a95a90a26b3 2025-10-07 Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.