Package 70518-3474-3

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3474-3
Digits Only 7051834743
Product NDC 70518-3474
Description

6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-3)

Marketing

Marketing Status
Marketed Since 2022-08-17
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": "37ec8e88-4c0e-8faa-e063-6294a90af75a", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["b09ca979-ab6b-441b-a66f-41ca32eae6cb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-2)", "package_ndc": "70518-3474-2", "marketing_start_date": "20220813"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-3)", "package_ndc": "70518-3474-3", "marketing_start_date": "20220817"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-4)", "package_ndc": "70518-3474-4", "marketing_start_date": "20220823"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-5)", "package_ndc": "70518-3474-5", "marketing_start_date": "20220823"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-7)", "package_ndc": "70518-3474-7", "marketing_start_date": "20220929"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-8)", "package_ndc": "70518-3474-8", "marketing_start_date": "20221109"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-9)", "package_ndc": "70518-3474-9", "marketing_start_date": "20221201"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "70518-3474_37ec8e88-4c0e-8faa-e063-6294a90af75a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3474", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20261231"}