Home NDC 87682-090-01 NDC 87682-090-01 - LANGLARA 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 87682-090
Requested NDC 87682-090-01
Package NDCs from labels 87682-090-01, 87682-090-05
Manufacturer Lanexa Biologics, LLC | Yichang HEC Changjiang Pharmaceutical Co.,Ltd.
Effective date 2026-10-15
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type LANGLARA Lanexa Biologics, LLC | Yichang HEC Changjiang Pharmaceutical Co.,Ltd. 2026-10-15 HUMAN PRESCRIPTION DRUG LABEL
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 155 of 226 · 4,512 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.