Package 70518-2611-3
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
70518-2611-3
Digits Only
7051826113
Product NDC
70518-2611
Description
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-3)
Marketing
Marketing Status
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": "4a79c032-6415-ec09-e063-6394a90a9967", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["f2eb32c3-3da0-4938-9ed9-ea8420450fde"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-3)", "package_ndc": "70518-2611-3", "marketing_start_date": "20241002"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-4)", "package_ndc": "70518-2611-4", "marketing_start_date": "20241108"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "70518-2611_4a79c032-6415-ec09-e063-6394a90a9967", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-2611", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20200303", "listing_expiration_date": "20271231"}