oxybutynin chloride

Generic: oxybutynin chloride

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler kvk-tech, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
KVK-Tech, Inc.

Identifiers & Regulatory

Product NDC 10702-201
Product ID 10702-201_289ec3ce-2fb1-608b-e063-6394a90a4a7a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209335
Listing Expiration 2026-12-31
Marketing Start 2017-12-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702201
Hyphenated Format 10702-201

Supplemental Identifiers

RxCUI
863664
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 ANDA209335 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (10702-201-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (10702-201-10)
  • 500 TABLET in 1 BOTTLE, PLASTIC (10702-201-50)
source: ndc

Packages (3)

10702-201-01 100 TABLET in 1 BOTTLE, PLASTIC (10702-201-01) 10702-201-10 1000 TABLET in 1 BOTTLE, PLASTIC (10702-201-10) 10702-201-50 500 TABLET in 1 BOTTLE, PLASTIC (10702-201-50)

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": "289ec3ce-2fb1-608b-e063-6394a90a4a7a", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["f99fdfe8-a980-4a72-bc99-aa2ce0bdfd86"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (10702-201-01)", "package_ndc": "10702-201-01", "marketing_start_date": "20171222"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (10702-201-10)", "package_ndc": "10702-201-10", "marketing_start_date": "20171222"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (10702-201-50)", "package_ndc": "10702-201-50", "marketing_start_date": "20171222"}], "brand_name": "Oxybutynin Chloride", "product_id": "10702-201_289ec3ce-2fb1-608b-e063-6394a90a4a7a", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "10702-201", "generic_name": "Oxybutynin Chloride", "labeler_name": "KVK-Tech, Inc.", "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"}