oxybutynin chloride

Generic: oxybutynin chloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1014
Product ID 71335-1014_d8012174-1a1c-46d9-9e97-094e9462a1f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209025
Listing Expiration 2026-12-31
Marketing Start 2018-02-01

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351014
Hyphenated Format 71335-1014

Supplemental Identifiers

RxCUI
863664
UNII
L9F3D9RENQ

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 ANDA209025 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1014-1)
  • 100 TABLET in 1 BOTTLE (71335-1014-2)
  • 20 TABLET in 1 BOTTLE (71335-1014-3)
  • 60 TABLET in 1 BOTTLE (71335-1014-4)
  • 90 TABLET in 1 BOTTLE (71335-1014-5)
  • 42 TABLET in 1 BOTTLE (71335-1014-6)
  • 15 TABLET in 1 BOTTLE (71335-1014-7)
  • 180 TABLET in 1 BOTTLE (71335-1014-8)
source: ndc

Packages (8)

Ingredients (1)

oxybutynin chloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d8012174-1a1c-46d9-9e97-094e9462a1f4", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["f26e590d-956e-493b-a6ac-6056aeeaf411"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1014-1)", "package_ndc": "71335-1014-1", "marketing_start_date": "20181121"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1014-2)", "package_ndc": "71335-1014-2", "marketing_start_date": "20240809"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1014-3)", "package_ndc": "71335-1014-3", "marketing_start_date": "20240809"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1014-4)", "package_ndc": "71335-1014-4", "marketing_start_date": "20240809"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1014-5)", "package_ndc": "71335-1014-5", "marketing_start_date": "20240809"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE (71335-1014-6)", "package_ndc": "71335-1014-6", "marketing_start_date": "20240809"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-1014-7)", "package_ndc": "71335-1014-7", "marketing_start_date": "20240809"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-1014-8)", "package_ndc": "71335-1014-8", "marketing_start_date": "20240809"}], "brand_name": "OXYBUTYNIN CHLORIDE", "product_id": "71335-1014_d8012174-1a1c-46d9-9e97-094e9462a1f4", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71335-1014", "generic_name": "OXYBUTYNIN CHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYBUTYNIN CHLORIDE", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209025", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}