Package 80425-0016-2

Brand: cyclobenzaprine hcl

Generic: cyclobenzaprine hcl
NDC Package

Package Facts

Identity

Package NDC 80425-0016-2
Digits Only 8042500162
Product NDC 80425-0016
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0016-2)

Marketing

Marketing Status
Marketed Since 2017-05-31
Brand cyclobenzaprine hcl
Generic cyclobenzaprine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a985779-947a-6d0e-e063-6294a90aa2a7", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["afca1267-4d8f-7453-e053-2995a90a865c"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0016-1)", "package_ndc": "80425-0016-1", "marketing_start_date": "20170531"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0016-2)", "package_ndc": "80425-0016-2", "marketing_start_date": "20170531"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0016-3)", "package_ndc": "80425-0016-3", "marketing_start_date": "20170531"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (80425-0016-4)", "package_ndc": "80425-0016-4", "marketing_start_date": "20170531"}], "brand_name": "Cyclobenzaprine HCL", "product_id": "80425-0016_2a985779-947a-6d0e-e063-6294a90aa2a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "80425-0016", "generic_name": "Cyclobenzaprine HCL", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine HCL", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}