Package 63459-701-60

Brand: amrix

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63459-701-60
Digits Only 6345970160
Product NDC 63459-701
Product ID 63459-701_ff33280b-7ccc-4a2e-bafd-cbc89cb1cee2
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63459-701-60)

Marketing

Marketing Status
Marketed Since 2007-11-01
Brand amrix
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

AMRIX ndc-match (0.95)

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 (63459-701-60)", "package_ndc": "63459-701-60", "marketing_start_date": "20071101"}], "brand_name": "AMRIX", "product_id": "63459-701_ff33280b-7ccc-4a2e-bafd-cbc89cb1cee2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63459-701", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Cephalon, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMRIX", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021777", "marketing_category": "NDA", "marketing_start_date": "20071001", "listing_expiration_date": "20261231"}