Home NDC 72162-2139-01 NDC 72162-2139-01 - Gabapentin 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 72162-2139
Requested NDC 72162-2139-01
Package NDCs from labels 72162-2139-1, 72162-2139-2, 72162-2139-3, 72162-2139-5, 72162-2139-9, 72162-2139-01
Manufacturer Bryant Ranch Prepack
Effective date 2024-10-18
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Gabapentin - Bryant Ranch Prepack Bryant Ranch Prepack 2024-10-18 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72162-2139-1 Gabapentin 100 in 1 BOTTLE, PLASTIC CAPSULE 100 104 72162-2139-2 Gabapentin 270 in 1 BOTTLE, PLASTIC CAPSULE 270 104 72162-2139-3 Gabapentin 30 in 1 BOTTLE, PLASTIC CAPSULE 30 104 72162-2139-5 Gabapentin 500 in 1 BOTTLE, PLASTIC CAPSULE 500 104 72162-2139-9 Gabapentin 90 in 1 BOTTLE, PLASTIC CAPSULE 90 104
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72162-2139 GABAPENTIN CAPSULE [BRYANT RANCH PREPACK] 104 Current NDC, 5 package rows 20241020_fb0b6613-57d6-4e24-946f-f5f87c460cf0.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 10 of 301 · 6,004 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.