oxybutynin chloride extended release
Generic: oxybutynin chloride
Labeler: avpakDrug Facts
Product Profile
Brand Name
oxybutynin chloride extended release
Generic Name
oxybutynin chloride
Labeler
avpak
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
oxybutynin chloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-628
Product ID
50268-628_32feb2f4-2ee5-6219-e063-6394a90a9ef9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078503
Listing Expiration
2026-12-31
Marketing Start
2012-05-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268628
Hyphenated Format
50268-628
Supplemental Identifiers
RxCUI
UNII
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 extended release (source: ndc)
Generic Name
oxybutynin chloride (source: ndc)
Application Number
ANDA078503 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-628-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-628-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32feb2f4-2ee5-6219-e063-6394a90a9ef9", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619", "863628", "863636"], "spl_set_id": ["242b4766-bc2b-0073-d72d-1bf879bbee24"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-628-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-628-11)", "package_ndc": "50268-628-15", "marketing_start_date": "20120525"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "50268-628_32feb2f4-2ee5-6219-e063-6394a90a9ef9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50268-628", "generic_name": "Oxybutynin Chloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078503", "marketing_category": "ANDA", "marketing_start_date": "20120525", "listing_expiration_date": "20261231"}