Package 82868-008-30

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-008-30
Digits Only 8286800830
Product NDC 82868-008
Product ID 82868-008_46dc8f32-6929-a243-e063-6394a90a19f8
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-008-30)

Marketing

Marketing Status
Marketed Since 2024-04-29
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46dc8f32-6929-a243-e063-6394a90a19f8", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["1912d134-a909-5511-e063-6294a90aea29"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-008-30)", "package_ndc": "82868-008-30", "marketing_start_date": "20240429"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "82868-008_46dc8f32-6929-a243-e063-6394a90a19f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "82868-008", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20240429", "listing_expiration_date": "20261231"}