oxybutynin chloride
Generic: oxybutynin chloride
Labeler: chartwell governmental & specialty rx, llc.Drug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
chartwell governmental & specialty rx, llc.
Dosage Form
SOLUTION
Routes
Active Ingredients
oxybutynin chloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68999-520
Product ID
68999-520_499c11a1-a248-9411-e063-6294a90a203a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075039
Listing Expiration
2027-12-31
Marketing Start
1999-01-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68999520
Hyphenated Format
68999-520
Supplemental Identifiers
RxCUI
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
ANDA075039 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 2 TRAY in 1 BOX (68999-520-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-520-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "499c11a1-a248-9411-e063-6294a90a203a", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863599"], "spl_set_id": ["46e78c72-a5a3-472f-9125-b120fa4eee31"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-520-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-520-05)", "package_ndc": "68999-520-24", "marketing_start_date": "20260128"}], "brand_name": "Oxybutynin Chloride", "product_id": "68999-520_499c11a1-a248-9411-e063-6294a90a203a", "dosage_form": "SOLUTION", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "68999-520", "generic_name": "Oxybutynin Chloride", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA075039", "marketing_category": "ANDA", "marketing_start_date": "19990129", "listing_expiration_date": "20271231"}