oxybutynin chloride extended release
Generic: oxybutynin chloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
oxybutynin chloride extended release
Generic Name
oxybutynin chloride
Labeler
american health packaging
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
oxybutynin chloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-610
Product ID
68084-610_230831a1-53bb-f16b-e063-6394a90ab9df
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078503
Listing Expiration
2026-12-31
Marketing Start
2012-12-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084610
Hyphenated Format
68084-610
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
- 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-610-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-610-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "230831a1-53bb-f16b-e063-6394a90ab9df", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619", "863636"], "spl_set_id": ["0c71bdfb-01db-49ac-a8e9-0037df0d24af"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-610-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-610-11)", "package_ndc": "68084-610-21", "marketing_start_date": "20121212"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "68084-610_230831a1-53bb-f16b-e063-6394a90ab9df", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "68084-610", "generic_name": "Oxybutynin Chloride", "labeler_name": "American Health Packaging", "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": "20121212", "listing_expiration_date": "20261231"}