Package 70518-4257-0

Brand: ramelteon

Generic: ramelteon
NDC Package

Package Facts

Identity

Package NDC 70518-4257-0
Digits Only 7051842570
Product NDC 70518-4257
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4257-0)

Marketing

Marketing Status
Marketed Since 2025-01-20
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": "4008bca7-b73b-5d1c-e063-6394a90a179b", "openfda": {"nui": ["N0000175743", "N0000000250"], "unii": ["901AS54I69"], "rxcui": ["577348"], "spl_set_id": ["5a3cf917-3569-4fc1-8b81-ffecfd2de005"], "pharm_class_epc": ["Melatonin Receptor Agonist [EPC]"], "pharm_class_moa": ["Melatonin Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4257-0)", "package_ndc": "70518-4257-0", "marketing_start_date": "20250120"}], "brand_name": "Ramelteon", "product_id": "70518-4257_4008bca7-b73b-5d1c-e063-6394a90a179b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Melatonin Receptor Agonist [EPC]", "Melatonin Receptor Agonists [MoA]"], "product_ndc": "70518-4257", "generic_name": "Ramelteon", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ramelteon", "active_ingredients": [{"name": "RAMELTEON", "strength": "8 mg/1"}], "application_number": "ANDA213815", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}