Package 71205-858-90
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
71205-858-90
Digits Only
7120585890
Product NDC
71205-858
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-90)
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": "ffd82a69-a64c-4399-8f5d-bddc70cdc3cf", "openfda": {"upc": ["0371205857301", "0371205858308"], "unii": ["0VE05JYS2P"], "rxcui": ["828353", "828358"], "spl_set_id": ["ffd82a69-a64c-4399-8f5d-bddc70cdc3cf"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-00)", "package_ndc": "71205-858-00", "marketing_start_date": "20220506"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-11)", "package_ndc": "71205-858-11", "marketing_start_date": "20220506"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-30)", "package_ndc": "71205-858-30", "marketing_start_date": "20220506"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-55)", "package_ndc": "71205-858-55", "marketing_start_date": "20220506"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-60)", "package_ndc": "71205-858-60", "marketing_start_date": "20220506"}, {"sample": false, "description": "120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-72)", "package_ndc": "71205-858-72", "marketing_start_date": "20220506"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-858-90)", "package_ndc": "71205-858-90", "marketing_start_date": "20220506"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71205-858_ffd82a69-a64c-4399-8f5d-bddc70cdc3cf", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71205-858", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Proficient Rx LP", "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": "20190301", "listing_expiration_date": "20261231"}