Package 80425-0203-1

Brand: ramelteon

Generic: ramelteon
NDC Package

Package Facts

Identity

Package NDC 80425-0203-1
Digits Only 8042502031
Product NDC 80425-0203
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0203-1)

Marketing

Marketing Status
Marketed Since 2020-06-30
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": "2a99c981-daf6-71e5-e063-6294a90a5c1d", "openfda": {"nui": ["N0000175743", "N0000000250"], "unii": ["901AS54I69"], "rxcui": ["577348"], "spl_set_id": ["ed37ac7c-ab7e-57b3-e053-2995a90a5b90"], "pharm_class_epc": ["Melatonin Receptor Agonist [EPC]"], "pharm_class_moa": ["Melatonin Receptor Agonists [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0203-1)", "package_ndc": "80425-0203-1", "marketing_start_date": "20200630"}], "brand_name": "Ramelteon", "product_id": "80425-0203_2a99c981-daf6-71e5-e063-6294a90a5c1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Melatonin Receptor Agonist [EPC]", "Melatonin Receptor Agonists [MoA]"], "product_ndc": "80425-0203", "generic_name": "Ramelteon", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "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": "20200630", "listing_expiration_date": "20261231"}