oxybutynin chloride

Generic: oxybutynin chloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxybutynin chloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-667
Product ID 71205-667_88f08450-559e-4038-aad1-051e4ab283cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207138
Listing Expiration 2026-12-31
Marketing Start 2016-12-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205667
Hyphenated Format 71205-667

Supplemental Identifiers

RxCUI
863619
UPC
0371205667306
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 ANDA207138 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)
source: ndc

Packages (3)

71205-667-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30) 71205-667-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60) 71205-667-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)

Ingredients (1)

oxybutynin chloride (10 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": "88f08450-559e-4038-aad1-051e4ab283cf", "openfda": {"upc": ["0371205667306"], "unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["88f08450-559e-4038-aad1-051e4ab283cf"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30)", "package_ndc": "71205-667-30", "marketing_start_date": "20220608"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60)", "package_ndc": "71205-667-60", "marketing_start_date": "20220608"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)", "package_ndc": "71205-667-90", "marketing_start_date": "20220608"}], "brand_name": "oxybutynin chloride", "product_id": "71205-667_88f08450-559e-4038-aad1-051e4ab283cf", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "71205-667", "generic_name": "oxybutynin chloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxybutynin chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207138", "marketing_category": "ANDA", "marketing_start_date": "20161220", "listing_expiration_date": "20261231"}