oxybutynin chloride
Generic: oxybutynin chloride
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
oxybutynin chloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
66267-642
Product ID
66267-642_1fa711ca-cee8-fae5-e063-6294a90aa5d0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209823
Listing Expiration
2026-12-31
Marketing Start
2017-11-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66267642
Hyphenated Format
66267-642
Supplemental Identifiers
RxCUI
UPC
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
ANDA209823 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (66267-642-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1fa711ca-cee8-fae5-e063-6294a90aa5d0", "openfda": {"upc": ["0366267642309"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["8e830697-a6d3-13ed-e053-2995a90acb11"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-642-30)", "package_ndc": "66267-642-30", "marketing_start_date": "20190725"}], "brand_name": "Oxybutynin Chloride", "product_id": "66267-642_1fa711ca-cee8-fae5-e063-6294a90aa5d0", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "66267-642", "generic_name": "Oxybutynin Chloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209823", "marketing_category": "ANDA", "marketing_start_date": "20171115", "listing_expiration_date": "20261231"}