oxybutynin

Generic: oxybutynin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin
Generic Name oxybutynin
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxybutynin chloride 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5353
Product ID 50090-5353_2d660e74-e22d-4493-9e7b-51c8031c3c69
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202332
Listing Expiration 2026-12-31
Marketing Start 2017-08-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905353
Hyphenated Format 50090-5353

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 (source: ndc)
Generic Name oxybutynin (source: ndc)
Application Number ANDA202332 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)
source: ndc

Packages (1)

50090-5353-0 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)

Ingredients (1)

oxybutynin chloride (10 mg/1)

Linked Drug Pages (1)

oxybutynin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d660e74-e22d-4493-9e7b-51c8031c3c69", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["1f95920c-5dc2-44e4-b61d-b2c5e05390ba"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)", "package_ndc": "50090-5353-0", "marketing_start_date": "20201111"}], "brand_name": "oxybutynin", "product_id": "50090-5353_2d660e74-e22d-4493-9e7b-51c8031c3c69", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-5353", "generic_name": "oxybutynin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxybutynin", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202332", "marketing_category": "ANDA", "marketing_start_date": "20170810", "listing_expiration_date": "20261231"}