armodafinil

Generic: armodafinil

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name armodafinil
Generic Name armodafinil
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 50 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-464
Product ID 72189-464_2c4dd8aa-05cd-69f7-e063-6294a90abcd1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206069
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-05-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189464
Hyphenated Format 72189-464

Supplemental Identifiers

RxCUI
724863
UNII
V63XWA605I

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 ANDA206069 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-464-30)
source: ndc

Packages (1)

72189-464-30 30 TABLET in 1 BOTTLE (72189-464-30)

Ingredients (1)

armodafinil (50 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": "2c4dd8aa-05cd-69f7-e063-6294a90abcd1", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724863"], "spl_set_id": ["facd329b-1925-61df-e053-6294a90ab738"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-464-30)", "package_ndc": "72189-464-30", "marketing_start_date": "20230503"}], "brand_name": "Armodafinil", "product_id": "72189-464_2c4dd8aa-05cd-69f7-e063-6294a90abcd1", "dosage_form": "TABLET", "product_ndc": "72189-464", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "50 mg/1"}], "application_number": "ANDA206069", "marketing_category": "ANDA", "marketing_start_date": "20230503", "listing_expiration_date": "20261231"}