Package 85509-1001-6

Brand: cyclobenzaprine hcl

Generic: cyclobenzaprine hcl
NDC Package

Package Facts

Identity

Package NDC 85509-1001-6
Digits Only 8550910016
Product NDC 85509-1001
Description

60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6)

Marketing

Marketing Status
Marketed Since 2025-07-21
Brand cyclobenzaprine hcl
Generic cyclobenzaprine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "488202dc-28f3-ad46-e063-6294a90a4238", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["3a397e88-d267-feed-e063-6294a90a7710"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (85509-1001-1)", "package_ndc": "85509-1001-1", "marketing_start_date": "20250721"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-1001-3)", "package_ndc": "85509-1001-3", "marketing_start_date": "20250721"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6)", "package_ndc": "85509-1001-6", "marketing_start_date": "20250721"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85509-1001-9)", "package_ndc": "85509-1001-9", "marketing_start_date": "20250721"}], "brand_name": "Cyclobenzaprine HCL", "product_id": "85509-1001_488202dc-28f3-ad46-e063-6294a90a4238", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "85509-1001", "generic_name": "Cyclobenzaprine HCL", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine HCL", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20150325", "listing_expiration_date": "20271231"}