Package 55154-2342-0

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-2342-0
Digits Only 5515423420
Product NDC 55154-2342
Product ID 55154-2342_4ab3f62d-40ab-4222-bf61-23c90df44aa6
Description

10 BLISTER PACK in 1 BAG (55154-2342-0) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-04-30
Brand duloxetine
Generic duloxetine hydrochloride
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": "4ab3f62d-40ab-4222-bf61-23c90df44aa6", "openfda": {"upc": ["0055154234108", "0055154234207"], "unii": ["9044SC542W"], "rxcui": ["596930", "596934"], "spl_set_id": ["26e7c5d9-f191-43d5-81c8-e6cf1fcb3986"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2342-0)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-2342-0", "marketing_end_date": "20260430", "marketing_start_date": "20131211"}], "brand_name": "Duloxetine", "product_id": "55154-2342_4ab3f62d-40ab-4222-bf61-23c90df44aa6", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "55154-2342", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090778", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20131211"}