Package 63629-1210-1

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1210-1
Digits Only 6362912101
Product NDC 63629-1210
Product ID 63629-1210_edc90a4b-ecb5-4bff-8e43-e4df262b42ee
Description

500 TABLET, FILM COATED in 1 BOTTLE (63629-1210-1)

Marketing

Marketing Status
Marketed Since 2021-01-14
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": "edc90a4b-ecb5-4bff-8e43-e4df262b42ee", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["aa29e260-fb77-415a-a505-3230d30c8945"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-1210-1)", "package_ndc": "63629-1210-1", "marketing_start_date": "20210114"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "63629-1210_edc90a4b-ecb5-4bff-8e43-e4df262b42ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63629-1210", "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": "10 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}