Package 76420-010-60

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-010-60
Digits Only 7642001060
Product NDC 76420-010
Description

60 TABLET, FILM COATED in 1 BOTTLE (76420-010-60)

Marketing

Marketing Status
Marketed Since 2020-01-23
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": "17d7186f-a791-93d2-e063-6294a90ac7d4", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["07e3ec53-f1f2-4231-aec6-1772a146ba88"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-010-01)", "package_ndc": "76420-010-01", "marketing_start_date": "20221021"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76420-010-05)", "package_ndc": "76420-010-05", "marketing_start_date": "20221021"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (76420-010-12)", "package_ndc": "76420-010-12", "marketing_start_date": "20230316"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (76420-010-15)", "package_ndc": "76420-010-15", "marketing_start_date": "20221021"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-010-30)", "package_ndc": "76420-010-30", "marketing_start_date": "20200123"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-010-60)", "package_ndc": "76420-010-60", "marketing_start_date": "20200123"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-010-90)", "package_ndc": "76420-010-90", "marketing_start_date": "20221021"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "76420-010_17d7186f-a791-93d2-e063-6294a90ac7d4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-010", "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": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20170928", "listing_expiration_date": "20261231"}