oxybutynin chloride
Generic: oxybutynin chloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
oxybutynin chloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-4622
Product ID
50090-4622_b50d393a-fbbf-4184-95a8-aadb8b0468f2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209335
Listing Expiration
2026-12-31
Marketing Start
2017-12-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904622
Hyphenated Format
50090-4622
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
ANDA209335 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-4622-0)
- 100 TABLET in 1 BOTTLE (50090-4622-1)
- 90 TABLET in 1 BOTTLE (50090-4622-3)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b50d393a-fbbf-4184-95a8-aadb8b0468f2", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["39a2d144-0c10-4aec-9fa4-0adc24b332eb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4622-0)", "package_ndc": "50090-4622-0", "marketing_start_date": "20191018"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-4622-1)", "package_ndc": "50090-4622-1", "marketing_start_date": "20191018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4622-3)", "package_ndc": "50090-4622-3", "marketing_start_date": "20191018"}], "brand_name": "Oxybutynin Chloride", "product_id": "50090-4622_b50d393a-fbbf-4184-95a8-aadb8b0468f2", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "50090-4622", "generic_name": "Oxybutynin Chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209335", "marketing_category": "ANDA", "marketing_start_date": "20171222", "listing_expiration_date": "20261231"}