Package 17856-0149-1

Brand: oxybutynin chloride

Generic: oxybutynin chloride
NDC Package

Package Facts

Identity

Package NDC 17856-0149-1
Digits Only 1785601491
Product NDC 17856-0149
Description

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0149-1) / 5 mL in 1 CUP, UNIT-DOSE

Marketing

Marketing Status
Marketed Since 2020-03-05
Brand oxybutynin chloride
Generic oxybutynin chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35cef500-044f-9368-e063-6294a90a9ae5", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863599"], "spl_set_id": ["fe4ed76b-0009-455f-be30-47e80fc1afdf"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0149-1)  / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-0149-1", "marketing_start_date": "20200305"}], "brand_name": "Oxybutynin Chloride", "product_id": "17856-0149_35cef500-044f-9368-e063-6294a90a9ae5", "dosage_form": "SYRUP", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "17856-0149", "generic_name": "Oxybutynin Chloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA074520", "marketing_category": "ANDA", "marketing_start_date": "19960329", "listing_expiration_date": "20261231"}