Package 71610-428-45
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
71610-428-45
Digits Only
7161042845
Product NDC
71610-428
Description
45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-428-45)
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": "437af220-8e2a-4629-899f-a4f7e85db5e7", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["be5201bc-e1f1-41af-be46-4a8fbb223b86"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-428-45)", "package_ndc": "71610-428-45", "marketing_start_date": "20200515"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71610-428_437af220-8e2a-4629-899f-a4f7e85db5e7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71610-428", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}