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 72789-490
Product ID 72789-490_2f24ff93-475c-5845-e063-6394a90a8faa
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 72789490
Hyphenated Format 72789-490

Supplemental Identifiers

RxCUI
863664
UPC
0372789490601
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
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-490-60)
source: ndc

Packages (1)

72789-490-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-490-60)

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": "2f24ff93-475c-5845-e063-6394a90a8faa", "openfda": {"upc": ["0372789490601"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["3a319017-4e25-402e-8ba0-63b9f1eb707e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-490-60)", "package_ndc": "72789-490-60", "marketing_start_date": "20250227"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "72789-490_2f24ff93-475c-5845-e063-6394a90a8faa", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72789-490", "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"}