Home NDC 73028-401-01 NDC 73028-401-01 - Hydrocortisone Acetate Pramoxine Hydrochloride 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 73028-401
Requested NDC 73028-401-01
Package NDCs from labels 73028-401-01, 73028-401-12
Manufacturer Pageview Pharmaceuticals
Effective date 2022-02-01
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73028-401-01 Hydrocortisone Acetate Pramoxine Hydrochloride 6 in 1 BLISTER PACK SUPPOSITORY 6 1 73028-401-12 Hydrocortisone Acetate Pramoxine Hydrochloride 2 in 1 BOX SUPPOSITORY 2 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73028-401 HYDROCORTISONE ACETATE PRAMOXINE HYDROCHLORIDE (HYDROCORTISONE ACETATE AND PRAMOXINE HYDROCHLORIDE) SUPPOSITORY [PAGEVIEW PHARMACEUTICALS] 1 Legacy NDC, 2 package rows 20220202_ac9617e7-0487-4ec8-8714-edcf967e9e50.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 19 of 19 · 362 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.