Home NDC 68308-784-01 NDC 68308-784-01 - Isotretinoin 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 68308-784
Requested NDC 68308-784-01
Package NDCs from labels 68308-784-01, 68308-784-30
Manufacturer Mayne Pharma
Effective date 2024-06-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Isotretinoin - Mayne Pharma Mayne Pharma 2024-06-26 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68308-784-01 Isotretinoin 10 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 10 4 68308-784-30 Isotretinoin 3 in 1 BOX CAPSULE, LIQUID FILLED 3 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68308-784 ISOTRETINOIN CAPSULE, LIQUID FILLED [MAYNE PHARMA] 4 Current NDC, 2 package rows 20240628_0114567b-3bac-490d-b9eb-03a6c5d90935.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 56 of 298 · 5,946 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.