Package 71335-2678-1

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2678-1
Digits Only 7133526781
Product NDC 71335-2678
Product ID 71335-2678_7e945c52-91dc-427d-a471-03fc6caac941
Description

5 TABLET, FILM COATED in 1 BOTTLE (71335-2678-1)

Marketing

Marketing Status
Marketed Since 2025-09-11
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": "7e945c52-91dc-427d-a471-03fc6caac941", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["cc93038f-1202-47f3-a959-2877877cc869"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (71335-2678-1)", "package_ndc": "71335-2678-1", "marketing_start_date": "20250911"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71335-2678_7e945c52-91dc-427d-a471-03fc6caac941", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71335-2678", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}