Package 50268-190-15

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-190-15
Digits Only 5026819015
Product NDC 50268-190
Product ID 50268-190_423d93a8-e8b9-b8a0-e063-6294a90a73be
Description

50 BLISTER PACK in 1 BOX (50268-190-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)

Marketing

Marketing Status
Marketed Since 2014-06-10
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "423d93a8-e8b9-b8a0-e063-6294a90a73be", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["64f6d1be-4067-a5c7-2343-4aed651a0cac"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-190-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)", "package_ndc": "50268-190-15", "marketing_start_date": "20140610"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "50268-190_423d93a8-e8b9-b8a0-e063-6294a90a73be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50268-190", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090478", "marketing_category": "ANDA", "marketing_start_date": "20140610", "listing_expiration_date": "20261231"}