bisacodyl
Generic: bisacodyl
Labeler: aphena pharma solutions - tennessee, llcDrug Facts
Product Profile
Brand Name
bisacodyl
Generic Name
bisacodyl
Labeler
aphena pharma solutions - tennessee, llc
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
bisacodyl 5 mg/1
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71610700
Hyphenated Format
71610-700
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
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)
Packages (6)
71610-700-02
2 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-02)
71610-700-03
3 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-03)
71610-700-04
4 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-04)
71610-700-06
6 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-06)
71610-700-08
8 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-08)
71610-700-20
20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71610-700-20)
Ingredients (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"}