Package 68382-255-06
Brand: oxybutynin
Generic: oxybutyninPackage Facts
Identity
Package NDC
68382-255-06
Digits Only
6838225506
Product NDC
68382-255
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-06)
Marketing
Marketing Status
Brand
oxybutynin
Generic
oxybutynin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f54e4d4e-91be-4e10-a446-57ed5e1843a1", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863619", "863628", "863636"], "spl_set_id": ["c042bf06-79a3-4dc7-ae05-3ef3cfae9d44"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-01)", "package_ndc": "68382-255-01", "marketing_start_date": "20170810"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-05)", "package_ndc": "68382-255-05", "marketing_start_date": "20170810"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-06)", "package_ndc": "68382-255-06", "marketing_start_date": "20170810"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-14)", "package_ndc": "68382-255-14", "marketing_start_date": "20170810"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-255-16)", "package_ndc": "68382-255-16", "marketing_start_date": "20170810"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-255-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-255-30)", "package_ndc": "68382-255-77", "marketing_start_date": "20170810"}], "brand_name": "oxybutynin", "product_id": "68382-255_f54e4d4e-91be-4e10-a446-57ed5e1843a1", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "68382-255", "generic_name": "oxybutynin", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxybutynin", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202332", "marketing_category": "ANDA", "marketing_start_date": "20170810", "listing_expiration_date": "20261231"}