Home NDC 70710-1775-00 NDC 70710-1775-00 - atorvastatin calcium 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 70710-1775
Requested NDC 70710-1775-00
Package NDCs from labels 70710-1775-9, 70710-1775-5, 70710-1775-0, 70710-1775-00
Manufacturer A-S Medication Solutions
Effective date 2025-10-21
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 70710-1775-0 atorvastatin calcium 1000 in 1 BOTTLE TABLET 1000 3 70710-1775-5 atorvastatin calcium 500 in 1 BOTTLE TABLET 500 3 70710-1775-9 atorvastatin calcium 90 in 1 BOTTLE TABLET 90 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70710-1775 ATORVASTATIN CALCIUM TABLET [ZYDUS PHARMACEUTICALS USA INC.] 2 Current NDC, 3 package rows 20240618_55ad4a90-d177-4cce-b7ec-cb75067f6c14.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 147 of 147 · 2,921 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TiZO2 TITANIUM DIOXIDE, ZINC OXIDE Fallien Cosmeceuticals, LTD. 30468afc-9616-4765-b046-12e97a0a7827 2010-12-20 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.