Package 16729-319-01
Brand: oxybutynin chloride
Generic: oxybutynin chloridePackage Facts
Identity
Package NDC
16729-319-01
Digits Only
1672931901
Product NDC
16729-319
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-319-01)
Marketing
Marketing Status
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": "461437aa-cf86-2475-e063-6294a90afe5b", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619", "863628", "863636"], "spl_set_id": ["61496a1e-17bf-4f45-a20c-5bb98fe545ee"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-319-01)", "package_ndc": "16729-319-01", "marketing_start_date": "20161214"}], "brand_name": "oxybutynin chloride", "product_id": "16729-319_461437aa-cf86-2475-e063-6294a90afe5b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "16729-319", "generic_name": "oxybutynin chloride", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxybutynin chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA207138", "marketing_category": "ANDA", "marketing_start_date": "20161214", "listing_expiration_date": "20261231"}