armodafinil

Generic: armodafinil

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name armodafinil
Generic Name armodafinil
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 250 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1308
Product ID 71335-1308_0c5145ed-6785-4545-b59e-dc5ba22a07dc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206069
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2018-03-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351308
Hyphenated Format 71335-1308

Supplemental Identifiers

RxCUI
724859 724861
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
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1308-1)
  • 28 TABLET in 1 BOTTLE (71335-1308-2)
  • 90 TABLET in 1 BOTTLE (71335-1308-3)
source: ndc

Packages (3)

71335-1308-1 30 TABLET in 1 BOTTLE (71335-1308-1) 71335-1308-2 28 TABLET in 1 BOTTLE (71335-1308-2) 71335-1308-3 90 TABLET in 1 BOTTLE (71335-1308-3)

Ingredients (1)

armodafinil (250 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": "0c5145ed-6785-4545-b59e-dc5ba22a07dc", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724859", "724861"], "spl_set_id": ["cbe7c0d9-dfd2-4000-bd76-7fe3454ce64f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1308-1)", "package_ndc": "71335-1308-1", "marketing_start_date": "20190823"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1308-2)", "package_ndc": "71335-1308-2", "marketing_start_date": "20190823"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1308-3)", "package_ndc": "71335-1308-3", "marketing_start_date": "20190823"}], "brand_name": "Armodafinil", "product_id": "71335-1308_0c5145ed-6785-4545-b59e-dc5ba22a07dc", "dosage_form": "TABLET", "product_ndc": "71335-1308", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "250 mg/1"}], "application_number": "ANDA206069", "marketing_category": "ANDA", "marketing_start_date": "20180306", "listing_expiration_date": "20261231"}