Package 70518-4246-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4246-0
Digits Only 7051842460
Product NDC 70518-4246
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4246-0)

Marketing

Marketing Status
Marketed Since 2024-12-23
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": "4007d5ed-c22b-1b06-e063-6294a90aa2f6", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828358"], "spl_set_id": ["30e61110-5bc8-4134-8456-538558479735"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4246-0)", "package_ndc": "70518-4246-0", "marketing_start_date": "20241223"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "70518-4246_4007d5ed-c22b-1b06-e063-6294a90aa2f6", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-4246", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "NDA021777", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20241223", "listing_expiration_date": "20261231"}