Package 72189-389-60

Brand: cyclobenzaprine hcl er

Generic: cyclobenzaprine hcl er
NDC Package

Package Facts

Identity

Package NDC 72189-389-60
Digits Only 7218938960
Product NDC 72189-389
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-389-60)

Marketing

Marketing Status
Marketed Since 2022-11-09
Brand cyclobenzaprine hcl er
Generic cyclobenzaprine hcl er
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cd6df-c359-b1f7-e063-6394a90a9507", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828358"], "spl_set_id": ["ed0b9acc-132f-64c0-e053-2995a90a198c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-389-60)", "package_ndc": "72189-389-60", "marketing_start_date": "20221109"}], "brand_name": "Cyclobenzaprine HCL ER", "product_id": "72189-389_2c4cd6df-c359-b1f7-e063-6394a90a9507", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72189-389", "generic_name": "Cyclobenzaprine HCL ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine HCL ER", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "NDA021777", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20221109", "listing_expiration_date": "20261231"}