Package 69306-075-09

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69306-075-09
Digits Only 6930607509
Product NDC 69306-075
Product ID 69306-075_cd092b93-57b8-bffc-e053-2a95a90a1a77
Description

90 TABLET, FILM COATED in 1 BOTTLE (69306-075-09)

Marketing

Marketing Status
Marketed Since 2021-01-15
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": "cd092b93-57b8-bffc-e053-2a95a90a1a77", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["64669718-02a0-47c6-9709-5f8db5736e04"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (69306-075-09)", "package_ndc": "69306-075-09", "marketing_start_date": "20210115"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "69306-075_cd092b93-57b8-bffc-e053-2a95a90a1a77", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "69306-075", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20180116", "listing_expiration_date": "20261231"}