Package 72162-1358-1
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
72162-1358-1
Digits Only
7216213581
Product NDC
72162-1358
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1358-1)
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": "8d5da604-8e13-492e-93d0-8f9890606e54", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["1e864da9-4004-484d-808b-01f826131a2b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1358-1)", "package_ndc": "72162-1358-1", "marketing_start_date": "20231003"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1358-5)", "package_ndc": "72162-1358-5", "marketing_start_date": "20231003"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "72162-1358_8d5da604-8e13-492e-93d0-8f9890606e54", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72162-1358", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}