Package 72162-1692-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1692-0
Digits Only 7216216920
Product NDC 72162-1692
Product ID 72162-1692_0208b80b-278d-4ef8-b9a2-858f77d9d789
Description

1000 TABLET, FILM COATED in 1 BOTTLE (72162-1692-0)

Marketing

Marketing Status
Marketed Since 2024-01-31
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": "0208b80b-278d-4ef8-b9a2-858f77d9d789", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["3f1b9c8a-8f75-4b84-af0c-739815937fd7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-1692-0)", "package_ndc": "72162-1692-0", "marketing_start_date": "20240131"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "72162-1692_0208b80b-278d-4ef8-b9a2-858f77d9d789", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72162-1692", "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"}