oxybutynin chloride

Generic: oxybutynin chloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-810
Product ID 23155-810_e12456ec-640f-45a5-b78a-66e22c36d24a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208165
Marketing Start 2022-01-31
Marketing End 2027-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155810
Hyphenated Format 23155-810

Supplemental Identifiers

RxCUI
863664
UPC
0323155810059 0323155810011 0323155810103
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
  • 100 TABLET in 1 BOTTLE (23155-810-01)
  • 500 TABLET in 1 BOTTLE (23155-810-05)
  • 1000 TABLET in 1 BOTTLE (23155-810-10)
source: ndc

Packages (3)

23155-810-01 100 TABLET in 1 BOTTLE (23155-810-01) 23155-810-05 500 TABLET in 1 BOTTLE (23155-810-05) 23155-810-10 1000 TABLET in 1 BOTTLE (23155-810-10)

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": "e12456ec-640f-45a5-b78a-66e22c36d24a", "openfda": {"upc": ["0323155810059", "0323155810011", "0323155810103"], "unii": ["L9F3D9RENQ"], "rxcui": ["863664"], "spl_set_id": ["9a551ec5-7e80-47c9-a7b9-f458c1478174"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-810-01)", "package_ndc": "23155-810-01", "marketing_end_date": "20270731", "marketing_start_date": "20220131"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-810-05)", "package_ndc": "23155-810-05", "marketing_end_date": "20270831", "marketing_start_date": "20220131"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-810-10)", "package_ndc": "23155-810-10", "marketing_end_date": "20270731", "marketing_start_date": "20220131"}], "brand_name": "Oxybutynin Chloride", "product_id": "23155-810_e12456ec-640f-45a5-b78a-66e22c36d24a", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "23155-810", "generic_name": "Oxybutynin Chloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "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_end_date": "20270831", "marketing_start_date": "20220131"}