Package 69097-846-15

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine
NDC Package

Package Facts

Identity

Package NDC 69097-846-15
Digits Only 6909784615
Product NDC 69097-846
Product ID 69097-846_0e5c376d-9599-4825-9226-016d40cf6113
Description

1000 TABLET, FILM COATED in 1 BOTTLE (69097-846-15)

Marketing

Marketing Status
Marketed Since 2016-07-22
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine
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": "0e5c376d-9599-4825-9226-016d40cf6113", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["575a31fb-04c5-4001-88a7-c33adbacc6a8"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69097-846-07)", "package_ndc": "69097-846-07", "marketing_start_date": "20160722"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69097-846-15)", "package_ndc": "69097-846-15", "marketing_start_date": "20160722"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "69097-846_0e5c376d-9599-4825-9226-016d40cf6113", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "69097-846", "generic_name": "Cyclobenzaprine", "labeler_name": "Cipla USA Inc.", "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"}