Package 82804-259-90

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-259-90
Digits Only 8280425990
Product NDC 82804-259
Description

90 TABLET, FILM COATED in 1 BOTTLE (82804-259-90)

Marketing

Marketing Status
Marketed Since 2025-12-30
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": "dfe7288c-a477-4f32-a9ab-00cc981a1a57", "openfda": {"upc": ["0382804259908"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["dfe7288c-a477-4f32-a9ab-00cc981a1a57"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-259-30)", "package_ndc": "82804-259-30", "marketing_start_date": "20251230"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82804-259-60)", "package_ndc": "82804-259-60", "marketing_start_date": "20251230"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-259-90)", "package_ndc": "82804-259-90", "marketing_start_date": "20251230"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "82804-259_dfe7288c-a477-4f32-a9ab-00cc981a1a57", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "82804-259", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20271231"}