Package 70518-3764-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3764-0
Digits Only 7051837640
Product NDC 70518-3764
Description

12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-0)

Marketing

Marketing Status
Marketed Since 2023-06-13
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": "3e493940-55c1-3f78-e063-6394a90a77c3", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["e4ed7ad2-cf58-4fdb-bc8c-d89f23b01210"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-0)", "package_ndc": "70518-3764-0", "marketing_start_date": "20230613"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-1)", "package_ndc": "70518-3764-1", "marketing_start_date": "20240305"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-2)", "package_ndc": "70518-3764-2", "marketing_start_date": "20250314"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "70518-3764_3e493940-55c1-3f78-e063-6394a90a77c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3764", "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": "20230613", "listing_expiration_date": "20261231"}