Package 68788-8522-3
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
68788-8522-3
Digits Only
6878885223
Product NDC
68788-8522
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8522-3)
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": "d7bcfd6d-30cd-4dc5-8fac-4298b7d4f3a9", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828358"], "spl_set_id": ["550d3e5a-c95f-4094-a500-1a02ea35a18d"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8522-3)", "package_ndc": "68788-8522-3", "marketing_start_date": "20230912"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68788-8522_d7bcfd6d-30cd-4dc5-8fac-4298b7d4f3a9", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-8522", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091281", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}