Package 50090-5712-8
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
50090-5712-8
Digits Only
5009057128
Product NDC
50090-5712
Description
6 TABLET, FILM COATED in 1 BOTTLE (50090-5712-8)
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": "39b5ac79-ad9a-4b68-ac00-f28408f7d31d", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["bf3c4c2e-b089-4f83-9c6a-7ca9d9abd3ba"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (50090-5712-0)", "package_ndc": "50090-5712-0", "marketing_start_date": "20210924"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (50090-5712-1)", "package_ndc": "50090-5712-1", "marketing_start_date": "20210924"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE (50090-5712-4)", "package_ndc": "50090-5712-4", "marketing_start_date": "20210924"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-5712-8)", "package_ndc": "50090-5712-8", "marketing_start_date": "20210924"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "50090-5712_39b5ac79-ad9a-4b68-ac00-f28408f7d31d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-5712", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}