oxybutynin chloride

Generic: oxybutynin chloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-277
Product ID 71610-277_b28dba2b-b19b-469e-98d8-54e87e3800e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209823
Listing Expiration 2026-12-31
Marketing Start 2017-10-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610277
Hyphenated Format 71610-277

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 ANDA209823 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71610-277-30)
  • 60 TABLET in 1 BOTTLE (71610-277-53)
  • 90 TABLET in 1 BOTTLE (71610-277-60)
  • 180 TABLET in 1 BOTTLE (71610-277-80)
  • 270 TABLET in 1 BOTTLE (71610-277-92)
source: ndc

Packages (5)

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": "b28dba2b-b19b-469e-98d8-54e87e3800e3", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["d2bb6927-5fbf-49ca-a891-d701bff1c812"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71610-277-30)", "package_ndc": "71610-277-30", "marketing_start_date": "20230531"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-277-53)", "package_ndc": "71610-277-53", "marketing_start_date": "20190513"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-277-60)", "package_ndc": "71610-277-60", "marketing_start_date": "20190513"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-277-80)", "package_ndc": "71610-277-80", "marketing_start_date": "20190513"}, {"sample": false, "description": "270 TABLET in 1 BOTTLE (71610-277-92)", "package_ndc": "71610-277-92", "marketing_start_date": "20190513"}], "brand_name": "Oxybutynin Chloride", "product_id": "71610-277_b28dba2b-b19b-469e-98d8-54e87e3800e3", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71610-277", "generic_name": "Oxybutynin Chloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, 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": "20171023", "listing_expiration_date": "20261231"}