Home NDC 71610-700-06 Bisacodyl
Product NDC 71610-700
Requested package NDC 71610-700-06
11-digit product format 716100700
Labeler code 71610
Product ID 71610-700_2b5b56c7-3f95-8a1c-e063-6394a90a4162
Type HUMAN OTC DRUG
Nonproprietary name Bisacodyl
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Aphena Pharma Solutions - Tennessee, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-12-01
Substance BISACODYL
Active strength 5 mg/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71610-700 71610-700-06 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Bisacodyl
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISACODYL 5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 10X0709Y6I Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308753 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71610-700-02 Bisacodyl 2 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 2 2 71610-700-03 Bisacodyl 3 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 3 2 71610-700-04 Bisacodyl 4 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 4 2 71610-700-06 Bisacodyl 6 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 6 2 71610-700-08 Bisacodyl 8 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 8 2 71610-700-20 Bisacodyl 20 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 20 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71610-700 BISACODYL TABLET, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] 2 Current NDC, 6 package rows 20250112_ca67d5e8-d67d-44ce-adf7-cf9b2eed89d2.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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 71610-700-06 71610070006 6 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-06) 2023-04-03 No No Current