bisacodyl

Generic: bisacodyl

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bisacodyl
Generic Name bisacodyl
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

bisacodyl 5 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-700
Product ID 71610-700_2b5b56c7-3f95-8a1c-e063-6394a90a4162
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2018-12-01

Pharmacologic Class

Established (EPC)
stimulant laxative [epc]
Physiologic Effect
increased large intestinal motility [pe] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610700
Hyphenated Format 71610-700

Supplemental Identifiers

RxCUI
308753
UNII
10X0709Y6I
NUI
N0000009371 N0000175812 N0000009871

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bisacodyl (source: ndc)
Generic Name bisacodyl (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 2 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-02)
  • 3 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-03)
  • 4 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-04)
  • 6 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-06)
  • 8 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-08)
  • 20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-20)
source: ndc

Packages (6)

Ingredients (1)

bisacodyl (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b5b56c7-3f95-8a1c-e063-6394a90a4162", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "unii": ["10X0709Y6I"], "rxcui": ["308753"], "spl_set_id": ["ca67d5e8-d67d-44ce-adf7-cf9b2eed89d2"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-02)", "package_ndc": "71610-700-02", "marketing_start_date": "20230403"}, {"sample": false, "description": "3 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-03)", "package_ndc": "71610-700-03", "marketing_start_date": "20230403"}, {"sample": false, "description": "4 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-04)", "package_ndc": "71610-700-04", "marketing_start_date": "20230403"}, {"sample": false, "description": "6 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-06)", "package_ndc": "71610-700-06", "marketing_start_date": "20230403"}, {"sample": false, "description": "8 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-08)", "package_ndc": "71610-700-08", "marketing_start_date": "20230403"}, {"sample": false, "description": "20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-20)", "package_ndc": "71610-700-20", "marketing_start_date": "20230403"}], "brand_name": "Bisacodyl", "product_id": "71610-700_2b5b56c7-3f95-8a1c-e063-6394a90a4162", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "71610-700", "generic_name": "Bisacodyl", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bisacodyl", "active_ingredients": [{"name": "BISACODYL", "strength": "5 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}