oxybutynin chloride
Generic: oxybutynin chloride
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
oxybutynin chloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82868-047
Product ID
82868-047_46dcbc0b-febf-ab63-e063-6394a90aee4c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209335
Listing Expiration
2026-12-31
Marketing Start
2024-02-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82868047
Hyphenated Format
82868-047
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 (source: ndc)
Generic Name
oxybutynin chloride (source: ndc)
Application Number
ANDA209335 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (82868-047-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46dcbc0b-febf-ab63-e063-6394a90aee4c", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["13a79659-a181-6a61-e063-6294a90ae034"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-047-30)", "package_ndc": "82868-047-30", "marketing_start_date": "20240219"}], "brand_name": "Oxybutynin Chloride", "product_id": "82868-047_46dcbc0b-febf-ab63-e063-6394a90aee4c", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "82868-047", "generic_name": "Oxybutynin Chloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209335", "marketing_category": "ANDA", "marketing_start_date": "20240219", "listing_expiration_date": "20261231"}