Package 72888-012-00
Brand: cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloridePackage Facts
Identity
Package NDC
72888-012-00
Digits Only
7288801200
Product NDC
72888-012
Description
1000 TABLET, FILM COATED in 1 BOTTLE (72888-012-00)
Marketing
Marketing Status
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": "484568be-57f8-943e-e063-6394a90a589b", "openfda": {"upc": ["0372888012001", "0372888012018", "0372888012056", "0372888014005", "0372888014050", "0372888013015", "0372888014012"], "unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["b2169957-9083-412c-a175-3071860c2b43"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72888-012-00)", "package_ndc": "72888-012-00", "marketing_start_date": "20211101"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-012-01)", "package_ndc": "72888-012-01", "marketing_start_date": "20170531"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72888-012-05)", "package_ndc": "72888-012-05", "marketing_start_date": "20170531"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "72888-012_484568be-57f8-943e-e063-6394a90a589b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72888-012", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Advagen Pharma Limited", "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"}