Package 60687-558-01

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine
NDC Package

Package Facts

Identity

Package NDC 60687-558-01
Digits Only 6068755801
Product NDC 60687-558
Description

100 BLISTER PACK in 1 CARTON (60687-558-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-558-11)

Marketing

Marketing Status
Marketed Since 2022-02-10
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": "437e4fe5-baf0-1534-e063-6394a90a22d4", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["269bc278-963d-4830-816a-39bb4bf8c936"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-558-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-558-11)", "package_ndc": "60687-558-01", "marketing_start_date": "20220210"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "60687-558_437e4fe5-baf0-1534-e063-6394a90a22d4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "60687-558", "generic_name": "Cyclobenzaprine", "labeler_name": "American Health Packaging", "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": "20220210", "listing_expiration_date": "20261231"}