oxybutynin chloride
Generic: oxybutynin chloride
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
oxybutynin chloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-665
Product ID
51655-665_4950ae3a-d3c8-b948-e063-6394a90afa44
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209823
Listing Expiration
2027-12-31
Marketing Start
2022-08-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655665
Hyphenated Format
51655-665
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 (source: ndc)
Generic Name
oxybutynin chloride (source: ndc)
Application Number
ANDA209823 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 60 TABLET in 1 BOTTLE, PLASTIC (51655-665-25)
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-665-52)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4950ae3a-d3c8-b948-e063-6394a90afa44", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["f330b7a0-bbe0-0f00-e053-2a95a90a37b8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-665-25)", "package_ndc": "51655-665-25", "marketing_start_date": "20221216"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-665-52)", "package_ndc": "51655-665-52", "marketing_start_date": "20220809"}], "brand_name": "Oxybutynin Chloride", "product_id": "51655-665_4950ae3a-d3c8-b948-e063-6394a90afa44", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "51655-665", "generic_name": "Oxybutynin Chloride", "labeler_name": "Northwind Health Company, LLC", "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": "20220809", "listing_expiration_date": "20271231"}