bisacodyl

Generic: bisacodyl

Labeler: kroger company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bisacodyl
Generic Name bisacodyl
Labeler kroger company
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

bisacodyl 5 mg/1

Manufacturer
KROGER COMPANY

Identifiers & Regulatory

Product NDC 41226-003
Product ID 41226-003_2dc61a4e-5307-5145-e063-6294a90a06d7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2020-06-01

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 41226003
Hyphenated Format 41226-003

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 M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 25 TABLET, COATED in 1 BLISTER PACK (41226-003-52)
source: ndc

Packages (1)

41226-003-52 25 TABLET, COATED in 1 BLISTER PACK (41226-003-52)

Ingredients (1)

bisacodyl (5 mg/1)

Linked Drug Pages (1)

Bisacodyl ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2dc61a4e-5307-5145-e063-6294a90a06d7", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "unii": ["10X0709Y6I"], "rxcui": ["308753"], "spl_set_id": ["a13a8eec-3652-8c57-e053-2995a90aaebf"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET, COATED in 1 BLISTER PACK (41226-003-52)", "package_ndc": "41226-003-52", "marketing_start_date": "20200601"}], "brand_name": "Bisacodyl", "product_id": "41226-003_2dc61a4e-5307-5145-e063-6294a90a06d7", "dosage_form": "TABLET, COATED", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "41226-003", "generic_name": "Bisacodyl", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bisacodyl", "active_ingredients": [{"name": "BISACODYL", "strength": "5 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}