Package 63459-700-60

Brand: amrix

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63459-700-60
Digits Only 6345970060
Product NDC 63459-700
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63459-700-60)

Marketing

Marketing Status
Marketed Since 2007-10-02
Brand amrix
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff33280b-7ccc-4a2e-bafd-cbc89cb1cee2", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828353", "828355", "828358", "828359"], "spl_set_id": ["3902123b-1365-ac3c-0934-afff9eeeb1bd"], "manufacturer_name": ["Cephalon, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63459-700-60)", "package_ndc": "63459-700-60", "marketing_start_date": "20071002"}], "brand_name": "AMRIX", "product_id": "63459-700_ff33280b-7ccc-4a2e-bafd-cbc89cb1cee2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63459-700", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Cephalon, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMRIX", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "NDA021777", "marketing_category": "NDA", "marketing_start_date": "20071002", "listing_expiration_date": "20261231"}