oxybutynin chloride

Generic: oxybutynin chloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-417
Product ID 72789-417_3ca468f2-1caa-f215-e063-6394a90aff4b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209025
Listing Expiration 2026-12-31
Marketing Start 2018-02-01

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789417
Hyphenated Format 72789-417

Supplemental Identifiers

RxCUI
863664
UPC
0372789417905
UNII
L9F3D9RENQ

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 oxybutynin chloride (source: ndc)
Generic Name oxybutynin chloride (source: ndc)
Application Number ANDA209025 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-417-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-417-90)
source: ndc

Packages (2)

72789-417-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-417-30) 72789-417-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-417-90)

Ingredients (1)

oxybutynin chloride (5 mg/1)

Linked Drug Pages (1)

OXYBUTYNIN CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ca468f2-1caa-f215-e063-6394a90aff4b", "openfda": {"upc": ["0372789417905"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["8bd5dce0-d56a-4e64-8de7-e7cd7775526b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-417-30)", "package_ndc": "72789-417-30", "marketing_start_date": "20250818"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-417-90)", "package_ndc": "72789-417-90", "marketing_start_date": "20240621"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "72789-417_3ca468f2-1caa-f215-e063-6394a90aff4b", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72789-417", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209025", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}