Package 65841-801-10
Brand: duloxetine
Generic: duloxetinePackage Facts
Identity
Package NDC
65841-801-10
Digits Only
6584180110
Product NDC
65841-801
Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-10)
Marketing
Marketing Status
Brand
duloxetine
Generic
duloxetine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "22968719-7127-4aab-b4c4-4497de16ca23", "openfda": {"upc": ["0365841800166", "0365841801163", "0365841799163"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["f36b414e-ace4-4f04-a80f-75bb25db430d"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-06)", "package_ndc": "65841-801-06", "marketing_start_date": "20140527"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-10)", "package_ndc": "65841-801-10", "marketing_start_date": "20140527"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-16)", "package_ndc": "65841-801-16", "marketing_start_date": "20140527"}], "brand_name": "Duloxetine", "product_id": "65841-801_22968719-7127-4aab-b4c4-4497de16ca23", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65841-801", "generic_name": "Duloxetine", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090739", "marketing_category": "ANDA", "marketing_start_date": "20140527", "listing_expiration_date": "20261231"}