ramelteon

Generic: ramelteon

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ramelteon
Generic Name ramelteon
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ramelteon 8 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1495
Product ID 70771-1495_5adaa941-43ea-41a8-944f-598d38132c99
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211567
Listing Expiration 2026-12-31
Marketing Start 2019-07-23

Pharmacologic Class

Established (EPC)
melatonin receptor agonist [epc]
Mechanism of Action
melatonin receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711495
Hyphenated Format 70771-1495

Supplemental Identifiers

RxCUI
577348
UNII
901AS54I69
NUI
N0000175743 N0000000250

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ramelteon (source: ndc)
Generic Name ramelteon (source: ndc)
Application Number ANDA211567 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70771-1495-1)
  • 30 TABLET in 1 BOTTLE (70771-1495-3)
  • 500 TABLET in 1 BOTTLE (70771-1495-5)
source: ndc

Packages (3)

70771-1495-1 100 TABLET in 1 BOTTLE (70771-1495-1) 70771-1495-3 30 TABLET in 1 BOTTLE (70771-1495-3) 70771-1495-5 500 TABLET in 1 BOTTLE (70771-1495-5)

Ingredients (1)

ramelteon (8 mg/1)

Linked Drug Pages (1)

Ramelteon ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5adaa941-43ea-41a8-944f-598d38132c99", "openfda": {"nui": ["N0000175743", "N0000000250"], "unii": ["901AS54I69"], "rxcui": ["577348"], "spl_set_id": ["14ba7994-476a-4978-8cac-29989335a63c"], "pharm_class_epc": ["Melatonin Receptor Agonist [EPC]"], "pharm_class_moa": ["Melatonin Receptor Agonists [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1495-1)", "package_ndc": "70771-1495-1", "marketing_start_date": "20190723"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1495-3)", "package_ndc": "70771-1495-3", "marketing_start_date": "20190723"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1495-5)", "package_ndc": "70771-1495-5", "marketing_start_date": "20190723"}], "brand_name": "Ramelteon", "product_id": "70771-1495_5adaa941-43ea-41a8-944f-598d38132c99", "dosage_form": "TABLET", "pharm_class": ["Melatonin Receptor Agonist [EPC]", "Melatonin Receptor Agonists [MoA]"], "product_ndc": "70771-1495", "generic_name": "Ramelteon", "labeler_name": "Zydus Lifesciences Limited", "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": "20190723", "listing_expiration_date": "20261231"}