Home NDC 70710-1401-03 NDC 70710-1401-03 - CLOBETASOL PROPIONATE 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 70710-1401
Requested NDC 70710-1401-03
Package NDCs from labels 70710-1401-1, 70710-1401-2, 70710-1401-4, 70710-1401-3, 70710-1401-03
Manufacturer Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited
Effective date 2022-10-05
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 70710-1401-1 CLOBETASOL PROPIONATE 1 in 1 CARTON OINTMENT 1 6 70710-1401-1 CLOBETASOL PROPIONATE 15 g in 1 TUBE OINTMENT 15 6 70710-1401-2 CLOBETASOL PROPIONATE 1 in 1 CARTON OINTMENT 1 6 70710-1401-2 CLOBETASOL PROPIONATE 30 g in 1 TUBE OINTMENT 30 6 70710-1401-3 CLOBETASOL PROPIONATE 60 g in 1 TUBE OINTMENT 60 6 70710-1401-3 CLOBETASOL PROPIONATE 1 in 1 CARTON OINTMENT 1 6 70710-1401-4 CLOBETASOL PROPIONATE 45 g in 1 TUBE OINTMENT 45 6 70710-1401-4 CLOBETASOL PROPIONATE 1 in 1 CARTON OINTMENT 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70710-1401 CLOBETASOL PROPIONATE OINTMENT [ZYDUS PHARMACEUTICALS USA INC.] 6 Current NDC, Legacy NDC, 8 package rows 20221007_98a25409-e84e-452b-8dc5-ad87842398e1.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 37 of 37 · 721 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.