oxybutynin chloride

Generic: oxybutynin chloride

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler direct rx
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxybutynin chloride 10 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-132
Product ID 72189-132_2bece08b-b60c-a15e-e063-6394a90a3a13
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207138
Listing Expiration 2026-12-31
Marketing Start 2020-08-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189132
Hyphenated Format 72189-132

Supplemental Identifiers

RxCUI
863619
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 ANDA207138 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)
source: ndc

Packages (1)

72189-132-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)

Ingredients (1)

oxybutynin chloride (10 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": "2bece08b-b60c-a15e-e063-6394a90a3a13", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["ada3be87-2cdd-75f7-e053-2995a90aa95b"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)", "package_ndc": "72189-132-30", "marketing_start_date": "20200824"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "72189-132_2bece08b-b60c-a15e-e063-6394a90a3a13", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72189-132", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207138", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}