armodafinil

Generic: armodafinil

Labeler: natco pharma usa llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name armodafinil
Generic Name armodafinil
Labeler natco pharma usa llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 200 mg/1

Manufacturer
Natco Pharma USA LLC

Identifiers & Regulatory

Product NDC 69339-179
Product ID 69339-179_d93dca81-a0da-49ee-be61-86e713ab56cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202768
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-03-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69339179
Hyphenated Format 69339-179

Supplemental Identifiers

RxCUI
724859 724861 724863 861960
UPC
0369339177105 0369339180051 0369339178102 0369339178034 0369339180037 0369339179031
UNII
V63XWA605I

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 armodafinil (source: ndc)
Generic Name armodafinil (source: ndc)
Application Number ANDA202768 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (69339-179-03)
  • 1000 TABLET in 1 BOTTLE (69339-179-10)
source: ndc

Packages (2)

69339-179-03 30 TABLET in 1 BOTTLE (69339-179-03) 69339-179-10 1000 TABLET in 1 BOTTLE (69339-179-10)

Ingredients (1)

armodafinil (200 mg/1)

Linked Drug Pages (1)

Armodafinil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d93dca81-a0da-49ee-be61-86e713ab56cd", "openfda": {"upc": ["0369339177105", "0369339180051", "0369339178102", "0369339178034", "0369339180037", "0369339179031"], "unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "861960"], "spl_set_id": ["de2f0921-e791-426c-9192-2b7162e2158c"], "manufacturer_name": ["Natco Pharma USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (69339-179-03)", "package_ndc": "69339-179-03", "marketing_start_date": "20230323"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69339-179-10)", "package_ndc": "69339-179-10", "marketing_start_date": "20230323"}], "brand_name": "Armodafinil", "product_id": "69339-179_d93dca81-a0da-49ee-be61-86e713ab56cd", "dosage_form": "TABLET", "product_ndc": "69339-179", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Natco Pharma USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "ANDA202768", "marketing_category": "ANDA", "marketing_start_date": "20230323", "listing_expiration_date": "20261231"}