Package 71205-678-30

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-678-30
Digits Only 7120567830
Product NDC 71205-678
Product ID 71205-678_e3998083-e3db-4052-9b5b-19d7aaa4e658
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-678-30)

Marketing

Marketing Status
Marketed Since 2022-07-27
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": "e3998083-e3db-4052-9b5b-19d7aaa4e658", "openfda": {"upc": ["0371205678609"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["e3998083-e3db-4052-9b5b-19d7aaa4e658"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-678-30)", "package_ndc": "71205-678-30", "marketing_start_date": "20220727"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-678-60)", "package_ndc": "71205-678-60", "marketing_start_date": "20220727"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-678-90)", "package_ndc": "71205-678-90", "marketing_start_date": "20220727"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71205-678_e3998083-e3db-4052-9b5b-19d7aaa4e658", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71205-678", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}