Home NDC 70710-1683-2 NDC 70710-1683-2 - 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 70710-1683
Requested NDC 70710-1683-2
Package NDCs from labels 70710-1683-3, 70710-1683-1, 70710-1683-5, 70710-1683-0, 70710-1683-2, 70710-1683-4
Manufacturer Safecor Health, LLC
Effective date 2026-06-11
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70710-1683-0 Famotidine 1000 in 1 BOTTLE TABLET, FILM COATED 1000 2 70710-1683-1 Famotidine 100 in 1 BOTTLE TABLET, FILM COATED 100 2 70710-1683-2 Famotidine 10 in 1 BLISTER PACK TABLET, FILM COATED 10 2 70710-1683-3 Famotidine 30 in 1 BOTTLE TABLET, FILM COATED 30 2 70710-1683-4 Famotidine 10 in 1 CARTON TABLET, FILM COATED 10 2 70710-1683-5 Famotidine 500 in 1 BOTTLE TABLET, FILM COATED 500 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70710-1683 FAMOTIDINE TABLET, FILM COATED [ZYDUS PHARMACEUTICALS USA INC.] 2 Current NDC, Legacy NDC, 6 package rows 20231011_b165979b-7ed0-423e-9aeb-2e061df0cd45.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 133 of 147 · 2,925 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.