Package 63629-2424-1

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2424-1
Digits Only 6362924241
Product NDC 63629-2424
Product ID 63629-2424_fb9eb346-51bf-4091-ab5b-56b40c763077
Description

1000 TABLET, FILM COATED in 1 BOTTLE (63629-2424-1)

Marketing

Marketing Status
Marketed Since 2021-02-25
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": "fb9eb346-51bf-4091-ab5b-56b40c763077", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["dcef9b63-f998-4852-920d-c356623cea6a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (63629-2424-1)", "package_ndc": "63629-2424-1", "marketing_start_date": "20210225"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "63629-2424_fb9eb346-51bf-4091-ab5b-56b40c763077", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63629-2424", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077563", "marketing_category": "ANDA", "marketing_start_date": "20060404", "listing_expiration_date": "20261231"}