oxybutynin chloride extended release
Generic: oxybutynin chloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
oxybutynin chloride extended release
Generic Name
oxybutynin chloride
Labeler
a-s medication solutions
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
oxybutynin chloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6673
Product ID
50090-6673_92090e0c-c4f0-420d-b3cf-cf54fcf219ff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206121
Listing Expiration
2027-12-31
Marketing Start
2016-09-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906673
Hyphenated Format
50090-6673
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
ANDA206121 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6673-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92090e0c-c4f0-420d-b3cf-cf54fcf219ff", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["3688227b-7655-40ca-b34b-073a39fd60f4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6673-0)", "package_ndc": "50090-6673-0", "marketing_start_date": "20230901"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "50090-6673_92090e0c-c4f0-420d-b3cf-cf54fcf219ff", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-6673", "generic_name": "Oxybutynin Chloride", "labeler_name": "A-S Medication Solutions", "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": "ANDA206121", "marketing_category": "ANDA", "marketing_start_date": "20160927", "listing_expiration_date": "20271231"}