oxybutynin chloride
Generic: oxybutynin chloride
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
redpharm drug
Dosage Form
TABLET
Routes
Active Ingredients
oxybutynin chloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-2045
Product ID
67296-2045_2c6318c6-0896-4b52-e063-6394a90a4e53
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212798
Listing Expiration
2026-12-31
Marketing Start
2019-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672962045
Hyphenated Format
67296-2045
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
ANDA212798 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (67296-2045-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c6318c6-0896-4b52-e063-6394a90a4e53", "openfda": {"upc": ["0369315182109", "0369315182055", "0369315182017"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["fc4cfbe6-a940-41c0-e053-6294a90adb14"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2045-3)", "package_ndc": "67296-2045-3", "marketing_start_date": "20191101"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "67296-2045_2c6318c6-0896-4b52-e063-6394a90a4e53", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "67296-2045", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212798", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}