Package 72189-369-30

Brand: ramelteon

Generic: ramelteon
NDC Package

Package Facts

Identity

Package NDC 72189-369-30
Digits Only 7218936930
Product NDC 72189-369
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-369-30)

Marketing

Marketing Status
Marketed Since 2022-08-03
Brand ramelteon
Generic ramelteon
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cb1fb-ac2c-e34f-e063-6294a90a33ef", "openfda": {"nui": ["N0000175743", "N0000000250"], "unii": ["901AS54I69"], "rxcui": ["577348"], "spl_set_id": ["e55aea01-80e6-60ae-e053-2995a90a9ca2"], "pharm_class_epc": ["Melatonin Receptor Agonist [EPC]"], "pharm_class_moa": ["Melatonin Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-369-30)", "package_ndc": "72189-369-30", "marketing_start_date": "20220803"}], "brand_name": "Ramelteon", "product_id": "72189-369_2c4cb1fb-ac2c-e34f-e063-6294a90a33ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Melatonin Receptor Agonist [EPC]", "Melatonin Receptor Agonists [MoA]"], "product_ndc": "72189-369", "generic_name": "Ramelteon", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ramelteon", "active_ingredients": [{"name": "RAMELTEON", "strength": "8 mg/1"}], "application_number": "ANDA212650", "marketing_category": "ANDA", "marketing_start_date": "20220803", "listing_expiration_date": "20261231"}