Package 72789-547-21

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-547-21
Digits Only 7278954721
Product NDC 72789-547
Product ID 72789-547_48ffe51b-f12a-2633-e063-6294a90aaae3
Description

21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-547-21)

Marketing

Marketing Status
Marketed Since 2026-01-12
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": "48ffe51b-f12a-2633-e063-6294a90aaae3", "openfda": {"upc": ["0372789547213"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["4eaa675a-c24c-4043-8fdf-9d59e5e4f4d5"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-547-21)", "package_ndc": "72789-547-21", "marketing_start_date": "20260112"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "72789-547_48ffe51b-f12a-2633-e063-6294a90aaae3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-547", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20271231"}