bisacodyl

Generic: bisacodyl

Labeler: chain drug consortium
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bisacodyl
Generic Name bisacodyl
Labeler chain drug consortium
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

bisacodyl 5 mg/1

Manufacturer
Chain Drug Consortium

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)
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 68016688
Hyphenated Format 68016-688

Supplemental Identifiers

RxCUI
308753
UNII
10X0709Y6I
NUI
N0000009371 N0000175812 N0000009871

Packaging Origin

Original Packager
true

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
  • 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
source: ndc

Packages (2)

Ingredients (1)

bisacodyl (5 mg/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"}