Package 72162-1359-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1359-0
Digits Only 7216213590
Product NDC 72162-1359
Description

1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-0)

Marketing

Marketing Status
Marketed Since 2024-01-31
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "720a5d84-521d-4a0f-a37b-cc0a6c7f2217", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["90c7a982-6442-4241-a60b-b5dfab2abb71"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-0)", "package_ndc": "72162-1359-0", "marketing_start_date": "20240131"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-1)", "package_ndc": "72162-1359-1", "marketing_start_date": "20240131"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-5)", "package_ndc": "72162-1359-5", "marketing_start_date": "20240131"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "72162-1359_720a5d84-521d-4a0f-a37b-cc0a6c7f2217", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72162-1359", "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"}