Package 60760-767-15

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-767-15
Digits Only 6076076715
Product NDC 60760-767
Description

15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-15)

Marketing

Marketing Status
Marketed Since 2023-06-08
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4472e8f6-6ee6-fc33-e063-6294a90a42c9", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["fe81c68d-a579-4fe9-e053-6294a90a7bc0"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-04)", "package_ndc": "60760-767-04", "marketing_start_date": "20230620"}, {"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-09)", "package_ndc": "60760-767-09", "marketing_start_date": "20230810"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-15)", "package_ndc": "60760-767-15", "marketing_start_date": "20230608"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-20)", "package_ndc": "60760-767-20", "marketing_start_date": "20230801"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-30)", "package_ndc": "60760-767-30", "marketing_start_date": "20230801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-90)", "package_ndc": "60760-767-90", "marketing_start_date": "20230707"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "60760-767_4472e8f6-6ee6-fc33-e063-6294a90a42c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "60760-767", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}