Package 76420-033-20

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-033-20
Digits Only 7642003320
Product NDC 76420-033
Description

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-20)

Marketing

Marketing Status
Marketed Since 2020-08-07
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f5f82b93-a80e-3ab8-e053-2995a90a68f5", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["68db3c3b-8da1-4852-90b0-3172f842aa02"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-01)", "package_ndc": "76420-033-01", "marketing_start_date": "20200807"}, {"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-02)", "package_ndc": "76420-033-02", "marketing_start_date": "20200807"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-07)", "package_ndc": "76420-033-07", "marketing_start_date": "20200807"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-20)", "package_ndc": "76420-033-20", "marketing_start_date": "20200807"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-30)", "package_ndc": "76420-033-30", "marketing_start_date": "20200807"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-60)", "package_ndc": "76420-033-60", "marketing_start_date": "20200807"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-033-90)", "package_ndc": "76420-033-90", "marketing_start_date": "20230303"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "76420-033_f5f82b93-a80e-3ab8-e053-2995a90a68f5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-033", "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": "10 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}