Package 67046-1645-3

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1645-3
Digits Only 6704616453
Product NDC 67046-1645
Product ID 67046-1645_47d22493-a548-559f-e063-6394a90a4126
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1645-3)

Marketing

Marketing Status
Marketed Since 2026-01-07
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": "47d22493-a548-559f-e063-6394a90a4126", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["47d22c6d-49fb-f97c-e063-6294a90a6ba1"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1645-3)", "package_ndc": "67046-1645-3", "marketing_start_date": "20260107"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "67046-1645_47d22493-a548-559f-e063-6394a90a4126", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67046-1645", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077563", "marketing_category": "ANDA", "marketing_start_date": "20260107", "listing_expiration_date": "20271231"}