Package 70518-4265-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4265-0
Digits Only 7051842650
Product NDC 70518-4265
Product ID 70518-4265_400a03ae-2ef6-c40f-e063-6394a90ae11a
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4265-0)

Marketing

Marketing Status
Marketed Since 2025-01-24
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": "400a03ae-2ef6-c40f-e063-6394a90ae11a", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["37056cab-953e-43ba-9b4c-163a739a52f7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4265-0)", "package_ndc": "70518-4265-0", "marketing_start_date": "20250124"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "70518-4265_400a03ae-2ef6-c40f-e063-6394a90ae11a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-4265", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20250124", "listing_expiration_date": "20261231"}