Package 67296-1893-3

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-1893-3
Digits Only 6729618933
Product NDC 67296-1893
Product ID 67296-1893_2c63f06e-644d-83aa-e063-6394a90a879a
Description

30 TABLET, FILM COATED in 1 BOTTLE (67296-1893-3)

Marketing

Marketing Status
Marketed Since 2008-09-26
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": "2c63f06e-644d-83aa-e063-6394a90a879a", "openfda": {"upc": ["0316571782017", "0316571783014"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["09d35c34-11fa-3a5d-e063-6294a90ab172"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-1893-3)", "package_ndc": "67296-1893-3", "marketing_start_date": "20080926"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "67296-1893_2c63f06e-644d-83aa-e063-6394a90a879a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67296-1893", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}