Package 68084-753-25

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-753-25
Digits Only 6808475325
Product NDC 68084-753
Product ID 68084-753_292934aa-0e3e-af97-e063-6394a90ae5b4
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-753-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-753-95)

Marketing

Marketing Status
Marketed Since 2016-01-04
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "292934aa-0e3e-af97-e063-6394a90ae5b4", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["5f321a03-ccfb-4c11-ac60-a461a5580c69"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-753-25)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-753-95)", "package_ndc": "68084-753-25", "marketing_start_date": "20160104"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (68084-753-65)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-753-11)", "package_ndc": "68084-753-65", "marketing_start_date": "20240327"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68084-753_292934aa-0e3e-af97-e063-6394a90ae5b4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68084-753", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078048", "marketing_category": "ANDA", "marketing_start_date": "20160104", "listing_expiration_date": "20261231"}