armodafinil

Generic: armodafinil

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

Drug Facts

Product Profile

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

armodafinil 50 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-8029
Product ID 0781-8029_dea0ad34-a35f-42ba-a6b6-dea58a16868f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021875
DEA Schedule civ
Marketing Start 2016-12-01
Marketing End 2027-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07818029
Hyphenated Format 0781-8029

Supplemental Identifiers

RxCUI
724859 724861 724863 861960
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 (0781-8029-31)
source: ndc

Packages (1)

0781-8029-31 30 TABLET in 1 BOTTLE (0781-8029-31)

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": "dea0ad34-a35f-42ba-a6b6-dea58a16868f", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "861960"], "spl_set_id": ["a3341ec8-1ad4-49e2-922b-13d1b30c8c1d"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0781-8029-31)", "package_ndc": "0781-8029-31", "marketing_end_date": "20270930", "marketing_start_date": "20161201"}], "brand_name": "Armodafinil", "product_id": "0781-8029_dea0ad34-a35f-42ba-a6b6-dea58a16868f", "dosage_form": "TABLET", "product_ndc": "0781-8029", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Sandoz 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": "20161201"}