oxybutynin chloride

Generic: oxybutynin chloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 50111-456
Product ID 50111-456_1811d8f0-3236-4dc7-a270-49e870188ff2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071655
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50111456
Hyphenated Format 50111-456

Supplemental Identifiers

RxCUI
863664
UPC
0350111456013
UNII
L9F3D9RENQ

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 oxybutynin chloride (source: ndc)
Generic Name oxybutynin chloride (source: ndc)
Application Number ANDA071655 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50111-456-01)
  • 500 TABLET in 1 BOTTLE (50111-456-02)
  • 1000 TABLET in 1 BOTTLE (50111-456-03)
source: ndc

Packages (3)

50111-456-01 100 TABLET in 1 BOTTLE (50111-456-01) 50111-456-02 500 TABLET in 1 BOTTLE (50111-456-02) 50111-456-03 1000 TABLET in 1 BOTTLE (50111-456-03)

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": "1811d8f0-3236-4dc7-a270-49e870188ff2", "openfda": {"upc": ["0350111456013"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["cb7aba8d-6913-4f57-8eb4-c6d6ff0b2a29"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50111-456-01)", "package_ndc": "50111-456-01", "marketing_start_date": "19900930"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50111-456-02)", "package_ndc": "50111-456-02", "marketing_start_date": "19900930"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (50111-456-03)", "package_ndc": "50111-456-03", "marketing_start_date": "19900930"}], "brand_name": "Oxybutynin Chloride", "product_id": "50111-456_1811d8f0-3236-4dc7-a270-49e870188ff2", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50111-456", "generic_name": "Oxybutynin Chloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA071655", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}