oxybutynin chloride

Generic: oxybutynin chloride

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

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6199
Product ID 50090-6199_ace59398-ff81-4474-9740-05c8594b28ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212798
Listing Expiration 2026-12-31
Marketing Start 2019-11-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906199
Hyphenated Format 50090-6199

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 ANDA212798 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6199-0)
  • 100 TABLET in 1 BOTTLE (50090-6199-1)
  • 90 TABLET in 1 BOTTLE (50090-6199-3)
source: ndc

Packages (3)

50090-6199-0 30 TABLET in 1 BOTTLE (50090-6199-0) 50090-6199-1 100 TABLET in 1 BOTTLE (50090-6199-1) 50090-6199-3 90 TABLET in 1 BOTTLE (50090-6199-3)

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": "ace59398-ff81-4474-9740-05c8594b28ac", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["83522acd-0ecc-46ac-a018-a3205ba096ff"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6199-0)", "package_ndc": "50090-6199-0", "marketing_start_date": "20221102"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6199-1)", "package_ndc": "50090-6199-1", "marketing_start_date": "20221102"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6199-3)", "package_ndc": "50090-6199-3", "marketing_start_date": "20221102"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "50090-6199_ace59398-ff81-4474-9740-05c8594b28ac", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-6199", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212798", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}