Package 76420-019-90

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-019-90
Digits Only 7642001990
Product NDC 76420-019
Product ID 76420-019_a73bd6a8-be64-4e54-e053-2a95a90a88a7
Description

90 TABLET, FILM COATED in 1 BOTTLE (76420-019-90)

Marketing

Marketing Status
Marketed Since 2020-06-04
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": "a73bd6a8-be64-4e54-e053-2a95a90a88a7", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["354286fa-7a64-4873-a188-14de8e86f677"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-019-30)", "package_ndc": "76420-019-30", "marketing_start_date": "20200604"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-019-60)", "package_ndc": "76420-019-60", "marketing_start_date": "20200604"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-019-90)", "package_ndc": "76420-019-90", "marketing_start_date": "20200604"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "76420-019_a73bd6a8-be64-4e54-e053-2a95a90a88a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-019", "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": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20180116", "listing_expiration_date": "20261231"}