Package 68788-8221-3

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8221-3
Digits Only 6878882213
Product NDC 68788-8221
Product ID 68788-8221_2c4631a2-3997-47ec-8914-59e78f30f6b1
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-8221-3)

Marketing

Marketing Status
Marketed Since 2022-09-09
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4631a2-3997-47ec-8914-59e78f30f6b1", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["29ca9548-23b0-4c50-82cb-4f0564d7e065"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8221-2)", "package_ndc": "68788-8221-2", "marketing_start_date": "20220909"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8221-3)", "package_ndc": "68788-8221-3", "marketing_start_date": "20220909"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8221-6)", "package_ndc": "68788-8221-6", "marketing_start_date": "20220909"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-8221-8)", "package_ndc": "68788-8221-8", "marketing_start_date": "20220909"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8221-9)", "package_ndc": "68788-8221-9", "marketing_start_date": "20220909"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68788-8221_2c4631a2-3997-47ec-8914-59e78f30f6b1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-8221", "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": "5 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20220909", "listing_expiration_date": "20261231"}