Package 70518-3415-6

Brand: CYCLOBENZAPRINE HYDROCHLORIDE

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3415-6
Digits Only 7051834156
Product NDC 70518-3415
Description

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-6)

Marketing

Marketing Status
Marketed Since 2024-09-24
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": "3effe04b-f23a-956d-e063-6394a90a0c3d", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["8bef97d4-1b92-4316-8733-7751d627230f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-1)", "package_ndc": "70518-3415-1", "marketing_start_date": "20240430"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-5)", "package_ndc": "70518-3415-5", "marketing_start_date": "20240918"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-6)", "package_ndc": "70518-3415-6", "marketing_start_date": "20240924"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "70518-3415_3effe04b-f23a-956d-e063-6394a90a0c3d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3415", "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": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20220429", "listing_expiration_date": "20261231"}