Package 68071-3567-2

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3567-2
Digits Only 6807135672
Product NDC 68071-3567
Description

12 TABLET, FILM COATED in 1 BOTTLE (68071-3567-2)

Marketing

Marketing Status
Marketed Since 2024-02-02
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "11d3bbb6-f6bd-0193-e063-6294a90a6957", "openfda": {"upc": ["0368071356731"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["106d9730-5938-8f27-e063-6294a90adc68"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (68071-3567-2)", "package_ndc": "68071-3567-2", "marketing_start_date": "20240202"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3567-3)", "package_ndc": "68071-3567-3", "marketing_start_date": "20240202"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "68071-3567_11d3bbb6-f6bd-0193-e063-6294a90a6957", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3567", "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": "5 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}