Package 70518-3287-2

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 70518-3287-2
Digits Only 7051832872
Product NDC 70518-3287
Product ID 70518-3287_468cb3e8-fecc-a2d1-e063-6294a90a8f4a
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-2)

Marketing

Marketing Status
Marketed Since 2025-05-28
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (1)

Duloxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "468cb3e8-fecc-a2d1-e063-6294a90a8f4a", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["ed164dbb-e713-42d1-a78e-31145578b9f8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-0)", "package_ndc": "70518-3287-0", "marketing_start_date": "20211209"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-2)", "package_ndc": "70518-3287-2", "marketing_start_date": "20250528"}], "brand_name": "Duloxetine", "product_id": "70518-3287_468cb3e8-fecc-a2d1-e063-6294a90a8f4a", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-3287", "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": "20211209", "listing_expiration_date": "20261231"}