Package 71610-933-45

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine
NDC Package

Package Facts

Identity

Package NDC 71610-933-45
Digits Only 7161093345
Product NDC 71610-933
Product ID 71610-933_3bc7e2c7-7cc9-adad-e063-6394a90ad5c4
Description

45 TABLET in 1 BOTTLE (71610-933-45)

Marketing

Marketing Status
Marketed Since 2025-08-06
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine
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": "3bc7e2c7-7cc9-adad-e063-6394a90ad5c4", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["3bc7e2b4-e1a0-66e3-e063-6294a90a676a"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE (71610-933-45)", "package_ndc": "71610-933-45", "marketing_start_date": "20250806"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "71610-933_3bc7e2c7-7cc9-adad-e063-6394a90ad5c4", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71610-933", "generic_name": "Cyclobenzaprine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090478", "marketing_category": "ANDA", "marketing_start_date": "20250410", "listing_expiration_date": "20261231"}