Package 51655-973-54

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine
NDC Package

Package Facts

Identity

Package NDC 51655-973-54
Digits Only 5165597354
Product NDC 51655-973
Description

15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54)

Marketing

Marketing Status
Marketed Since 2022-08-24
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4960a71d-10d7-6f03-e063-6394a90a710f", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["e04eea45-12ec-4d2b-e053-2a95a90a6b76"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-20)", "package_ndc": "51655-973-20", "marketing_start_date": "20221017"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-25)", "package_ndc": "51655-973-25", "marketing_start_date": "20220906"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-52)", "package_ndc": "51655-973-52", "marketing_start_date": "20221007"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-53)", "package_ndc": "51655-973-53", "marketing_start_date": "20220727"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54)", "package_ndc": "51655-973-54", "marketing_start_date": "20220824"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-87)", "package_ndc": "51655-973-87", "marketing_start_date": "20220504"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "51655-973_4960a71d-10d7-6f03-e063-6394a90a710f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "51655-973", "generic_name": "Cyclobenzaprine", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090478", "marketing_category": "ANDA", "marketing_start_date": "20220504", "listing_expiration_date": "20271231"}