Package 50090-6864-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6864-0
Digits Only 5009068640
Product NDC 50090-6864
Product ID 50090-6864_e077578e-bfb6-4b2b-a41f-9a0f272244db
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6864-0)

Marketing

Marketing Status
Marketed Since 2023-12-04
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

CYCLOBENZAPRINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e077578e-bfb6-4b2b-a41f-9a0f272244db", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["d6448bb1-9b8d-45f4-a14b-8328248e586e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6864-0)", "package_ndc": "50090-6864-0", "marketing_start_date": "20231204"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "50090-6864_e077578e-bfb6-4b2b-a41f-9a0f272244db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-6864", "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": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}