Package 70518-1244-2
Brand: duloxetine
Generic: duloxetinePackage Facts
Identity
Package NDC
70518-1244-2
Digits Only
7051812442
Product NDC
70518-1244
Description
180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-2)
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": "4af0d7e3-80e8-11e0-e063-6294a90a494d", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["461d769c-b787-4bc7-b4a6-7a5f33ae9d45"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-0)", "package_ndc": "70518-1244-0", "marketing_start_date": "20180605"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-1)", "package_ndc": "70518-1244-1", "marketing_start_date": "20250324"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-2)", "package_ndc": "70518-1244-2", "marketing_start_date": "20250416"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-3)", "package_ndc": "70518-1244-3", "marketing_start_date": "20251209"}], "brand_name": "Duloxetine", "product_id": "70518-1244_4af0d7e3-80e8-11e0-e063-6294a90a494d", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1244", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20180605", "listing_expiration_date": "20271231"}