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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5822
Product ID 50090-5822_0266855a-dbf4-4258-92c5-51e8c0a0738c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207138
Listing Expiration 2026-12-31
Marketing Start 2016-12-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905822
Hyphenated Format 50090-5822

Supplemental Identifiers

RxCUI
863636
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
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-0)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-1)
source: ndc

Packages (2)

50090-5822-0 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-0) 50090-5822-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-1)

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": "0266855a-dbf4-4258-92c5-51e8c0a0738c", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863636"], "spl_set_id": ["7593becc-250f-4d25-8401-a9f72f3f5ad4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-0)", "package_ndc": "50090-5822-0", "marketing_start_date": "20211020"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-1)", "package_ndc": "50090-5822-1", "marketing_start_date": "20230719"}], "brand_name": "oxybutynin chloride", "product_id": "50090-5822_0266855a-dbf4-4258-92c5-51e8c0a0738c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-5822", "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": "ANDA207138", "marketing_category": "ANDA", "marketing_start_date": "20161214", "listing_expiration_date": "20261231"}