Package 55154-0190-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-0190-0
Digits Only 5515401900
Product NDC 55154-0190
Description

10 BLISTER PACK in 1 BAG (55154-0190-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "df902d94-9d2b-4139-aebb-3eb6b8b8cd54", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["df902d94-9d2b-4139-aebb-3eb6b8b8cd54"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-0190-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-0190-0", "marketing_start_date": "20251010"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "55154-0190_df902d94-9d2b-4139-aebb-3eb6b8b8cd54", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "55154-0190", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20251010", "listing_expiration_date": "20261231"}