oxybutynin chloride extended release

Generic: oxybutynin chloride

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

Drug Facts

Product Profile

Brand Name oxybutynin chloride extended release
Generic Name oxybutynin chloride
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxybutynin chloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2121
Product ID 71335-2121_9b4a7465-5a1a-4474-b2d3-9befee70bc1c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206121
Listing Expiration 2026-12-31
Marketing Start 2016-09-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352121
Hyphenated Format 71335-2121

Supplemental Identifiers

RxCUI
863619
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 extended release (source: ndc)
Generic Name oxybutynin chloride (source: ndc)
Application Number ANDA206121 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1)
  • 18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-2)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-4)
source: ndc

Packages (4)

71335-2121-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1) 71335-2121-2 18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-2) 71335-2121-3 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-3) 71335-2121-4 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-4)

Ingredients (1)

oxybutynin chloride (10 mg/1)

Linked Drug Pages (1)

Oxybutynin Chloride Extended Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9b4a7465-5a1a-4474-b2d3-9befee70bc1c", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["169d6d58-8887-4bdd-95bd-873d1f049eaa"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1)", "package_ndc": "71335-2121-1", "marketing_start_date": "20220620"}, {"sample": false, "description": "18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-2)", "package_ndc": "71335-2121-2", "marketing_start_date": "20220620"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-3)", "package_ndc": "71335-2121-3", "marketing_start_date": "20220620"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-4)", "package_ndc": "71335-2121-4", "marketing_start_date": "20220620"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "71335-2121_9b4a7465-5a1a-4474-b2d3-9befee70bc1c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71335-2121", "generic_name": "Oxybutynin Chloride", "labeler_name": "Bryant Ranch Prepack", "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": "20261231"}