armodafinil

Generic: armodafinil

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name armodafinil
Generic Name armodafinil
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 50 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-3090
Product ID 0093-3090_ca66f83d-4d17-4516-9163-abdb19872555
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021875
DEA Schedule civ
Marketing Start 2016-11-29
Marketing End 2027-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00933090
Hyphenated Format 0093-3090

Supplemental Identifiers

RxCUI
724859 724861 724863 861960
UPC
0300933093569 0300933094566 0300933090568
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 NDA021875 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (0093-3090-56)
source: ndc

Packages (1)

0093-3090-56 30 TABLET in 1 BOTTLE (0093-3090-56)

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": "ca66f83d-4d17-4516-9163-abdb19872555", "openfda": {"upc": ["0300933093569", "0300933094566", "0300933090568"], "unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "861960"], "spl_set_id": ["b3cac300-c3d2-4189-a410-2aaf3773c090"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0093-3090-56)", "package_ndc": "0093-3090-56", "marketing_end_date": "20270930", "marketing_start_date": "20161129"}], "brand_name": "Armodafinil", "product_id": "0093-3090_ca66f83d-4d17-4516-9163-abdb19872555", "dosage_form": "TABLET", "product_ndc": "0093-3090", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "50 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20270930", "marketing_start_date": "20161129"}