Package 68788-9967-9
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
68788-9967-9
Digits Only
6878899679
Product NDC
68788-9967
Description
90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9)
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": "00f58c32-e17f-472d-8499-2e9d974146c3", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["a4cc7965-2ba8-42e8-8c5c-b90145a6598a"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-9967-1)", "package_ndc": "68788-9967-1", "marketing_start_date": "20150501"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-9967-2)", "package_ndc": "68788-9967-2", "marketing_start_date": "20150501"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-9967-3)", "package_ndc": "68788-9967-3", "marketing_start_date": "20150501"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6)", "package_ndc": "68788-9967-6", "marketing_start_date": "20150501"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE (68788-9967-7)", "package_ndc": "68788-9967-7", "marketing_start_date": "20190814"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-9967-8)", "package_ndc": "68788-9967-8", "marketing_start_date": "20150501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9)", "package_ndc": "68788-9967-9", "marketing_start_date": "20150501"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68788-9967_00f58c32-e17f-472d-8499-2e9d974146c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-9967", "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": "7.5 mg/1"}], "application_number": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20150501", "listing_expiration_date": "20261231"}