Package 72189-153-30

Brand: ramelteon

Generic: ramelteon
NDC Package

Package Facts

Identity

Package NDC 72189-153-30
Digits Only 7218915330
Product NDC 72189-153
Description

30 TABLET in 1 BOTTLE (72189-153-30)

Marketing

Marketing Status
Marketed Since 2020-11-03
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": "2be9051e-225a-8882-e063-6294a90a543a", "openfda": {"nui": ["N0000175743", "N0000000250"], "unii": ["901AS54I69"], "rxcui": ["577348"], "spl_set_id": ["b336438f-7951-d3b7-e053-2995a90a4d69"], "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 in 1 BOTTLE (72189-153-30)", "package_ndc": "72189-153-30", "marketing_start_date": "20201103"}], "brand_name": "RAMELTEON", "product_id": "72189-153_2be9051e-225a-8882-e063-6294a90a543a", "dosage_form": "TABLET", "pharm_class": ["Melatonin Receptor Agonist [EPC]", "Melatonin Receptor Agonists [MoA]"], "product_ndc": "72189-153", "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": "ANDA211567", "marketing_category": "ANDA", "marketing_start_date": "20201103", "listing_expiration_date": "20261231"}