Package 76420-265-60
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
76420-265-60
Digits Only
7642026560
Product NDC
76420-265
Description
60 TABLET, FILM COATED in 1 BOTTLE (76420-265-60)
Marketing
Marketing Status
Brand
cyclobenzaprine hydrochloride
Generic
cyclobenzaprine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e89c4c80-d10f-2a48-e053-2995a90a5d58", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["2a6b2ad9-307a-4976-98b7-1b96e0408da7"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-265-10)", "package_ndc": "76420-265-10", "marketing_start_date": "20220901"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-265-30)", "package_ndc": "76420-265-30", "marketing_start_date": "20220901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-265-60)", "package_ndc": "76420-265-60", "marketing_start_date": "20220901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-265-90)", "package_ndc": "76420-265-90", "marketing_start_date": "20220901"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "76420-265_e89c4c80-d10f-2a48-e053-2995a90a5d58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-265", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}