Package 68071-3561-6

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3561-6
Digits Only 6807135616
Product NDC 68071-3561
Product ID 68071-3561_149278a3-d3a4-c55b-e063-6294a90ab196
Description

9 TABLET, FILM COATED in 1 BOTTLE (68071-3561-6)

Marketing

Marketing Status
Marketed Since 2024-01-02
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": "149278a3-d3a4-c55b-e063-6294a90ab196", "openfda": {"upc": ["0368071356168"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["0f8ba2c0-38e7-a536-e063-6294a90ace8d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-3561-4)", "package_ndc": "68071-3561-4", "marketing_start_date": "20240102"}, {"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (68071-3561-6)", "package_ndc": "68071-3561-6", "marketing_start_date": "20240102"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "68071-3561_149278a3-d3a4-c55b-e063-6294a90ab196", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3561", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}