armodafinil

Generic: armodafinil

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name armodafinil
Generic Name armodafinil
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 200 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7826
Product ID 68788-7826_8f3858c1-8fd9-49cf-a1fa-e4d11d4ce86b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206069
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2021-01-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887826
Hyphenated Format 68788-7826

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 ANDA206069 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-7826-3)
  • 60 TABLET in 1 BOTTLE (68788-7826-6)
  • 90 TABLET in 1 BOTTLE (68788-7826-9)
source: ndc

Packages (3)

68788-7826-3 30 TABLET in 1 BOTTLE (68788-7826-3) 68788-7826-6 60 TABLET in 1 BOTTLE (68788-7826-6) 68788-7826-9 90 TABLET in 1 BOTTLE (68788-7826-9)

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": "8f3858c1-8fd9-49cf-a1fa-e4d11d4ce86b", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["861960"], "spl_set_id": ["93b9f9a4-66d9-4ed9-8f2f-903e416e900d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7826-3)", "package_ndc": "68788-7826-3", "marketing_start_date": "20210105"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7826-6)", "package_ndc": "68788-7826-6", "marketing_start_date": "20210105"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7826-9)", "package_ndc": "68788-7826-9", "marketing_start_date": "20210105"}], "brand_name": "Armodafinil", "product_id": "68788-7826_8f3858c1-8fd9-49cf-a1fa-e4d11d4ce86b", "dosage_form": "TABLET", "product_ndc": "68788-7826", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "ANDA206069", "marketing_category": "ANDA", "marketing_start_date": "20210105", "listing_expiration_date": "20271231"}