Package 43063-790-90
Brand: oxybutynin chloride extended release
Generic: oxybutynin chloridePackage Facts
Identity
Package NDC
43063-790-90
Digits Only
4306379090
Product NDC
43063-790
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-790-90)
Marketing
Marketing Status
Brand
oxybutynin chloride extended release
Generic
oxybutynin chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "419e3f00-a475-03d5-e063-6394a90a5f89", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619"], "spl_set_id": ["b5653b7e-1e3b-4da3-b3a2-33318f448c67"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-790-90)", "package_ndc": "43063-790-90", "marketing_start_date": "20170921"}], "brand_name": "Oxybutynin Chloride Extended Release", "product_id": "43063-790_419e3f00-a475-03d5-e063-6394a90a5f89", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "43063-790", "generic_name": "Oxybutynin Chloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078503", "marketing_category": "ANDA", "marketing_start_date": "20090301", "listing_expiration_date": "20261231"}