Package 50268-191-15

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine
NDC Package

Package Facts

Identity

Package NDC 50268-191-15
Digits Only 5026819115
Product NDC 50268-191
Description

50 BLISTER PACK in 1 BOX (50268-191-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-191-11)

Marketing

Marketing Status
Marketed Since 2022-08-01
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "423db048-ad6b-f3a9-e063-6394a90a192c", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["e530fd1e-06fd-0432-e053-2995a90adf5f"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-191-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-191-11)", "package_ndc": "50268-191-15", "marketing_start_date": "20220801"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "50268-191_423db048-ad6b-f3a9-e063-6394a90a192c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50268-191", "generic_name": "Cyclobenzaprine", "labeler_name": "AvPAK", "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": "20220801", "listing_expiration_date": "20261231"}