bisacodyl
Generic: bisacodyl
Labeler: chain drug consortiumDrug Facts
Product Profile
Brand Name
bisacodyl
Generic Name
bisacodyl
Labeler
chain drug consortium
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
bisacodyl 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68016-688
Product ID
68016-688_12bba10e-970d-443e-93fe-796395cc7093
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Marketing Start
2002-03-25
Marketing End
2027-01-31
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68016688
Hyphenated Format
68016-688
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-688-10) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
- 1 BLISTER PACK in 1 CARTON (68016-688-25) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "12bba10e-970d-443e-93fe-796395cc7093", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "unii": ["10X0709Y6I"], "rxcui": ["308753"], "spl_set_id": ["71215710-f33d-4e01-a543-fc46b5ce5137"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-688-10) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "68016-688-10", "marketing_end_date": "20270131", "marketing_start_date": "20020325"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68016-688-25) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "68016-688-25", "marketing_end_date": "20270131", "marketing_start_date": "20020325"}], "brand_name": "Bisacodyl", "product_id": "68016-688_12bba10e-970d-443e-93fe-796395cc7093", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "68016-688", "generic_name": "Bisacodyl", "labeler_name": "Chain Drug Consortium", "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_end_date": "20270131", "marketing_start_date": "20020325"}