Package 70518-1054-9
Brand: duloxetine
Generic: duloxetinePackage Facts
Identity
Package NDC
70518-1054-9
Digits Only
7051810549
Product NDC
70518-1054
Description
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-9)
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": "4af0f952-aef1-1a5e-e063-6394a90a41b2", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["b149641a-03e6-4fee-91f3-7ba8e01196bd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-0)", "package_ndc": "70518-1054-0", "marketing_start_date": "20180309"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-6)", "package_ndc": "70518-1054-6", "marketing_start_date": "20210609"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-7)", "package_ndc": "70518-1054-7", "marketing_start_date": "20210625"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-9)", "package_ndc": "70518-1054-9", "marketing_start_date": "20211202"}], "brand_name": "Duloxetine", "product_id": "70518-1054_4af0f952-aef1-1a5e-e063-6394a90a41b2", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1054", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20180309", "listing_expiration_date": "20271231"}