Package 0615-8084-05
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprinePackage Facts
Identity
Package NDC
0615-8084-05
Digits Only
0615808405
Product NDC
0615-8084
Description
15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-05)
Marketing
Marketing Status
Brand
cyclobenzaprine hydrochloride
Generic
cyclobenzaprine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3af92905-fa00-41fa-9156-037f58b21a0b", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["53688de9-2031-4d19-b422-4000285f7f47"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-05)", "package_ndc": "0615-8084-05", "marketing_start_date": "20160722"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-39)", "package_ndc": "0615-8084-39", "marketing_start_date": "20160722"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "0615-8084_3af92905-fa00-41fa-9156-037f58b21a0b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0615-8084", "generic_name": "Cyclobenzaprine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090478", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}