Package 68071-4655-2

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4655-2
Digits Only 6807146552
Product NDC 68071-4655
Product ID 68071-4655_48364978-c5f5-6e2c-e063-6394a90a593a
Description

12 TABLET, FILM COATED in 1 BOTTLE (68071-4655-2)

Marketing

Marketing Status
Marketed Since 2018-12-07
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": "48364978-c5f5-6e2c-e063-6394a90a593a", "openfda": {"upc": ["0368071465532"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["7c732db1-8321-82a4-e053-2991aa0aa8a0"], "manufacturer_name": ["NuCare Pharmaceutuicals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (68071-4655-2)", "package_ndc": "68071-4655-2", "marketing_start_date": "20181207"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4655-3)", "package_ndc": "68071-4655-3", "marketing_start_date": "20181207"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "68071-4655_48364978-c5f5-6e2c-e063-6394a90a593a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-4655", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "NuCare Pharmaceutuicals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20271231"}