Package 80425-0017-1

Brand: cyclobenzaprine hcl

Generic: cyclobenzaprine hcl
NDC Package

Package Facts

Identity

Package NDC 80425-0017-1
Digits Only 8042500171
Product NDC 80425-0017
Product ID 80425-0017_2a982dd7-c533-0a5b-e063-6294a90aafd3
Description

60 TABLET, FILM COATED in 1 BOTTLE (80425-0017-1)

Marketing

Marketing Status
Marketed Since 2006-04-04
Brand cyclobenzaprine hcl
Generic cyclobenzaprine hcl
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a982dd7-c533-0a5b-e063-6294a90aafd3", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["afca2a49-6424-7b6a-e053-2a95a90ad41e"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0017-1)", "package_ndc": "80425-0017-1", "marketing_start_date": "20060404"}], "brand_name": "Cyclobenzaprine HCL", "product_id": "80425-0017_2a982dd7-c533-0a5b-e063-6294a90aafd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "80425-0017", "generic_name": "Cyclobenzaprine HCL", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine HCL", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077563", "marketing_category": "ANDA", "marketing_start_date": "20060404", "listing_expiration_date": "20261231"}