bisacodyl

Generic: bisacodyl

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bisacodyl
Generic Name bisacodyl
Labeler major pharmaceuticals
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

bisacodyl 5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6748
Product ID 0904-6748_14fafe89-e4bf-4282-8a72-3bfcee7227fc
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 09046748
Hyphenated Format 0904-6748

Supplemental Identifiers

RxCUI
308753
UPC
0309046748809
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 BLISTER PACK in 1 CARTON (0904-6748-17) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-60)
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-80)
source: ndc

Packages (3)

0904-6748-17 1 BLISTER PACK in 1 CARTON (0904-6748-17) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK 0904-6748-60 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-60) 0904-6748-80 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-80)

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": "14fafe89-e4bf-4282-8a72-3bfcee7227fc", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "upc": ["0309046748809"], "unii": ["10X0709Y6I"], "rxcui": ["308753"], "spl_set_id": ["6b85af55-35db-4630-8bc0-9ff4fbf5990a"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0904-6748-17)  / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6748-17", "marketing_start_date": "20181201"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-60)", "package_ndc": "0904-6748-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0904-6748-80)", "package_ndc": "0904-6748-80", "marketing_start_date": "20181201"}], "brand_name": "Bisacodyl", "product_id": "0904-6748_14fafe89-e4bf-4282-8a72-3bfcee7227fc", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0904-6748", "generic_name": "Bisacodyl", "labeler_name": "Major Pharmaceuticals", "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"}