Package 64980-705-01

Brand: fexmid

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64980-705-01
Digits Only 6498070501
Product NDC 64980-705
Description

100 TABLET in 1 BOTTLE (64980-705-01)

Marketing

Marketing Status
Marketed Since 2025-03-10
Brand fexmid
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8ebfc7eb-5a9a-4f3d-af2c-370732df074f", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299", "828301"], "spl_set_id": ["41838966-de0b-4855-83b8-2ff6c764ed1f"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-705-01)", "package_ndc": "64980-705-01", "marketing_start_date": "20250310"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64980-705-50)", "package_ndc": "64980-705-50", "marketing_start_date": "20250310"}], "brand_name": "Fexmid", "product_id": "64980-705_8ebfc7eb-5a9a-4f3d-af2c-370732df074f", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "64980-705", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fexmid", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA218936", "marketing_category": "ANDA", "marketing_start_date": "20250310", "listing_expiration_date": "20261231"}