armodafinil

Generic: armodafinil

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

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

armodafinil 200 mg/1

Manufacturer
DirectRx

Identifiers & Regulatory

Product NDC 72189-353
Product ID 72189-353_2c4c8cee-041f-c5ef-e063-6394a90a8cfd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021875
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2022-04-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189353
Hyphenated Format 72189-353

Supplemental Identifiers

RxCUI
861960
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 NDA021875 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-353-30)
source: ndc

Packages (1)

72189-353-30 30 TABLET in 1 BOTTLE (72189-353-30)

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": "2c4c8cee-041f-c5ef-e063-6394a90a8cfd", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["861960"], "spl_set_id": ["ddd06dab-0855-5b4e-e053-2a95a90a5e67"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-353-30)", "package_ndc": "72189-353-30", "marketing_start_date": "20220429"}], "brand_name": "ARMODAFINIL", "product_id": "72189-353_2c4c8cee-041f-c5ef-e063-6394a90a8cfd", "dosage_form": "TABLET", "product_ndc": "72189-353", "dea_schedule": "CIV", "generic_name": "ARMODAFINIL", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARMODAFINIL", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220429", "listing_expiration_date": "20261231"}