Package 70518-4440-0

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4440-0
Digits Only 7051844400
Product NDC 70518-4440
Product ID 70518-4440_3c53fdd6-1d4b-530d-e063-6294a90aed43
Description

30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-4440-0)

Marketing

Marketing Status
Marketed Since 2025-08-14
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c53fdd6-1d4b-530d-e063-6294a90aed43", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["c66fb2ee-f64a-4d28-a692-e8dc7b61fbc9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-4440-0)", "package_ndc": "70518-4440-0", "marketing_start_date": "20250814"}], "brand_name": "Duloxetine", "product_id": "70518-4440_3c53fdd6-1d4b-530d-e063-6294a90aed43", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4440", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20250814", "listing_expiration_date": "20261231"}