Package 63629-1212-1

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1212-1
Digits Only 6362912121
Product NDC 63629-1212
Product ID 63629-1212_c000dfb8-781e-41aa-84eb-2fe5dad1bc77
Description

500 TABLET, FILM COATED in 1 BOTTLE (63629-1212-1)

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": "c000dfb8-781e-41aa-84eb-2fe5dad1bc77", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["8b58cd96-1371-441f-b38c-5b18dde98bbc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-1212-1)", "package_ndc": "63629-1212-1", "marketing_start_date": "20210114"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "63629-1212_c000dfb8-781e-41aa-84eb-2fe5dad1bc77", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63629-1212", "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": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}