Package 76420-256-60

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-256-60
Digits Only 7642025660
Product NDC 76420-256
Product ID 76420-256_e425b6aa-1438-785f-e053-2a95a90a4350
Description

60 TABLET, FILM COATED in 1 BOTTLE (76420-256-60)

Marketing

Marketing Status
Marketed Since 2022-07-19
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": "e425b6aa-1438-785f-e053-2a95a90a4350", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["59945ea1-8136-4014-acd9-cdfe6e11e8da"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-256-30)", "package_ndc": "76420-256-30", "marketing_start_date": "20220719"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-256-60)", "package_ndc": "76420-256-60", "marketing_start_date": "20220719"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-256-90)", "package_ndc": "76420-256-90", "marketing_start_date": "20220719"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "76420-256_e425b6aa-1438-785f-e053-2a95a90a4350", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-256", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}