Package 82461-714-90

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82461-714-90
Digits Only 8246171490
Product NDC 82461-714
Product ID 82461-714_24fbbff2-fec1-4884-8dfc-1d19a20d5f0d
Description

90 TABLET, FILM COATED in 1 BOTTLE (82461-714-90)

Marketing

Marketing Status
Marketed Since 2026-01-11
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

CYCLOBENZAPRINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24fbbff2-fec1-4884-8dfc-1d19a20d5f0d", "openfda": {"upc": ["0382461714901", "0382461716905"], "unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["1b834bd5-9ee6-42a4-819c-5c605fd18e1f"], "manufacturer_name": ["Medcore LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82461-714-90)", "package_ndc": "82461-714-90", "marketing_start_date": "20260111"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "82461-714_24fbbff2-fec1-4884-8dfc-1d19a20d5f0d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "82461-714", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Medcore LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20260111", "listing_expiration_date": "20271231"}