Package 0002-3240-30
Brand: cymbalta
Generic: duloxetine hydrochloridePackage Facts
Identity
Package NDC
0002-3240-30
Digits Only
0002324030
Product NDC
0002-3240
Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-30)
Marketing
Marketing Status
Brand
cymbalta
Generic
duloxetine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aa5061b1-f237-425a-9d05-575c333dfd37", "openfda": {"upc": ["0300023270306", "0300023240309", "0300023235602"], "unii": ["9044SC542W"], "rxcui": ["596926", "596928", "596930", "596932", "596934", "615186"], "spl_set_id": ["2f7d4d67-10c1-4bf4-a7f2-c185fbad64ba"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-30)", "package_ndc": "0002-3240-30", "marketing_end_date": "20260417", "marketing_start_date": "20040824"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-90)", "package_ndc": "0002-3240-90", "marketing_end_date": "20260417", "marketing_start_date": "20040824"}], "brand_name": "Cymbalta", "product_id": "0002-3240_aa5061b1-f237-425a-9d05-575c333dfd37", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0002-3240", "generic_name": "Duloxetine hydrochloride", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cymbalta", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021427", "marketing_category": "NDA", "marketing_end_date": "20261002", "marketing_start_date": "20040824"}