Package 70518-4523-0
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
70518-4523-0
Digits Only
7051845230
Product NDC
70518-4523
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4523-0)
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": "44e68141-7279-de8a-e063-6294a90a79d2", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828353"], "spl_set_id": ["fada6577-bcb8-422c-be37-08562919ebc9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4523-0)", "package_ndc": "70518-4523-0", "marketing_start_date": "20251125"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "70518-4523_44e68141-7279-de8a-e063-6294a90a79d2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-4523", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA091281", "marketing_category": "ANDA", "marketing_start_date": "20251125", "listing_expiration_date": "20261231"}