Package 50090-5772-0

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5772-0
Digits Only 5009057720
Product NDC 50090-5772
Product ID 50090-5772_338e97bd-601c-4c69-b1a2-aadcb9dd1c36
Description

15 TABLET, FILM COATED in 1 BOTTLE (50090-5772-0)

Marketing

Marketing Status
Marketed Since 2021-10-06
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "338e97bd-601c-4c69-b1a2-aadcb9dd1c36", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["f3187074-6b55-44a3-b969-40a808eb034a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-5772-0)", "package_ndc": "50090-5772-0", "marketing_start_date": "20211006"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "50090-5772_338e97bd-601c-4c69-b1a2-aadcb9dd1c36", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-5772", "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": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}