oxybutynin chloride

Generic: oxybutynin chloride

Labeler: strides pharma science limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler strides pharma science limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
Strides Pharma Science Limited

Identifiers & Regulatory

Product NDC 64380-781
Product ID 64380-781_c26252c5-9f52-4ef1-a7e1-79fff8ab7e6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208165
Listing Expiration 2026-12-31
Marketing Start 2024-12-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64380781
Hyphenated Format 64380-781

Supplemental Identifiers

RxCUI
863664
UPC
0364380781066 0364380781073 0364380781080
UNII
L9F3D9RENQ

Packaging Origin

Original Packager
true

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 ANDA208165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (64380-781-03)
  • 90 TABLET in 1 BOTTLE (64380-781-05)
  • 100 TABLET in 1 BOTTLE (64380-781-06)
  • 500 TABLET in 1 BOTTLE (64380-781-07)
  • 1000 TABLET in 1 BOTTLE (64380-781-08)
source: ndc

Packages (5)

64380-781-03 60 TABLET in 1 BOTTLE (64380-781-03) 64380-781-05 90 TABLET in 1 BOTTLE (64380-781-05) 64380-781-06 100 TABLET in 1 BOTTLE (64380-781-06) 64380-781-07 500 TABLET in 1 BOTTLE (64380-781-07) 64380-781-08 1000 TABLET in 1 BOTTLE (64380-781-08)

Ingredients (1)

oxybutynin chloride (5 mg/1)

Linked Drug Pages (1)

Oxybutynin Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c26252c5-9f52-4ef1-a7e1-79fff8ab7e6c", "openfda": {"upc": ["0364380781066", "0364380781073", "0364380781080"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["ac10c7b7-d0cb-4068-93e2-c0e51f15866e"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (64380-781-03)", "package_ndc": "64380-781-03", "marketing_start_date": "20241220"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (64380-781-05)", "package_ndc": "64380-781-05", "marketing_start_date": "20241220"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (64380-781-06)", "package_ndc": "64380-781-06", "marketing_start_date": "20241220"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64380-781-07)", "package_ndc": "64380-781-07", "marketing_start_date": "20241220"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64380-781-08)", "package_ndc": "64380-781-08", "marketing_start_date": "20241220"}], "brand_name": "Oxybutynin Chloride", "product_id": "64380-781_c26252c5-9f52-4ef1-a7e1-79fff8ab7e6c", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "64380-781", "generic_name": "Oxybutynin Chloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208165", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}