oxybutynin chloride

Generic: oxybutynin chloride

Labeler: verityrx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler verityrx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
VERITYRX, LLC

Identifiers & Regulatory

Product NDC 83939-0022
Product ID 83939-0022_427b8d8e-0187-6ba0-e063-6294a90ac52b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209823
Listing Expiration 2026-12-31
Marketing Start 2017-11-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 839390022
Hyphenated Format 83939-0022

Supplemental Identifiers

RxCUI
863664
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 ANDA209823 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 TABLET in 1 POUCH (83939-0022-1)
  • 50 POUCH in 1 BOX, UNIT-DOSE (83939-0022-2) / 1 TABLET in 1 POUCH
  • 100 POUCH in 1 BOX, UNIT-DOSE (83939-0022-3) / 1 TABLET in 1 POUCH
source: ndc

Packages (3)

83939-0022-1 1 TABLET in 1 POUCH (83939-0022-1) 83939-0022-2 50 POUCH in 1 BOX, UNIT-DOSE (83939-0022-2) / 1 TABLET in 1 POUCH 83939-0022-3 100 POUCH in 1 BOX, UNIT-DOSE (83939-0022-3) / 1 TABLET in 1 POUCH

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": "427b8d8e-0187-6ba0-e063-6294a90ac52b", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["427b6ffb-3ff4-932f-e063-6394a90ae8b9"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 POUCH (83939-0022-1)", "package_ndc": "83939-0022-1", "marketing_start_date": "20251103"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0022-2)  / 1 TABLET in 1 POUCH", "package_ndc": "83939-0022-2", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (83939-0022-3)  / 1 TABLET in 1 POUCH", "package_ndc": "83939-0022-3", "marketing_start_date": "20251103"}], "brand_name": "Oxybutynin Chloride", "product_id": "83939-0022_427b8d8e-0187-6ba0-e063-6294a90ac52b", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "83939-0022", "generic_name": "Oxybutynin Chloride", "labeler_name": "VERITYRX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209823", "marketing_category": "ANDA", "marketing_start_date": "20171115", "listing_expiration_date": "20261231"}