Package 67296-1441-1

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-1441-1
Digits Only 6729614411
Product NDC 67296-1441
Product ID 67296-1441_2c6228e2-dbac-01e7-e063-6394a90acbbc
Description

10 TABLET, FILM COATED in 1 BOTTLE (67296-1441-1)

Marketing

Marketing Status
Marketed Since 2020-07-06
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": "2c6228e2-dbac-01e7-e063-6394a90acbbc", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["09d0e2fc-76a4-bb7d-e063-6394a90a4a7d"], "manufacturer_name": ["Redpharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (67296-1441-1)", "package_ndc": "67296-1441-1", "marketing_start_date": "20200706"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "67296-1441_2c6228e2-dbac-01e7-e063-6394a90acbbc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67296-1441", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "Redpharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}