oxybutynin chloride
Generic: oxybutynin chloride
Labeler: trupharma llcDrug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
trupharma llc
Dosage Form
TABLET
Routes
Active Ingredients
oxybutynin chloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
52817-260
Product ID
52817-260_edabf40d-d160-c14b-e053-2995a90af00d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210125
Listing Expiration
2026-12-31
Marketing Start
2019-01-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52817260
Hyphenated Format
52817-260
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA210125 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (52817-260-10)
- 500 TABLET in 1 BOTTLE, PLASTIC (52817-260-50)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edabf40d-d160-c14b-e053-2995a90af00d", "openfda": {"upc": ["0352817260109"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["7c497c6c-2448-2c80-e053-2991aa0ab8c7"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (52817-260-10)", "package_ndc": "52817-260-10", "marketing_start_date": "20190101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (52817-260-50)", "package_ndc": "52817-260-50", "marketing_start_date": "20190101"}], "brand_name": "Oxybutynin Chloride", "product_id": "52817-260_edabf40d-d160-c14b-e053-2995a90af00d", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "52817-260", "generic_name": "oxybutynin chloride", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210125", "marketing_category": "ANDA", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}