modafinil
Generic: modafinil
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
modafinil
Generic Name
modafinil
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
modafinil 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
23155-862
Product ID
23155-862_d8fc4961-6cbc-44fc-be5f-63127fff98f8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207196
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2024-02-21
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155862
Hyphenated Format
23155-862
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
modafinil (source: ndc)
Generic Name
modafinil (source: ndc)
Application Number
ANDA207196 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (23155-862-01)
- 30 TABLET in 1 BOTTLE (23155-862-03)
- 500 TABLET in 1 BOTTLE (23155-862-05)
- 90 TABLET in 1 BOTTLE (23155-862-09)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d8fc4961-6cbc-44fc-be5f-63127fff98f8", "openfda": {"nui": ["N0000175729", "N0000175651", "N0000175769"], "upc": ["0323155605037", "0323155862010", "0323155862034", "0323155604030", "0323155862058", "0323155604092", "0323155605099", "0323155862096"], "unii": ["R3UK8X3U3D"], "rxcui": ["205324", "260218"], "spl_set_id": ["1a309416-bd6a-45b1-982f-b689b097453d"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]"], "pharm_class_epc": ["Sympathomimetic-like Agent [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-862-01)", "package_ndc": "23155-862-01", "marketing_start_date": "20240221"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (23155-862-03)", "package_ndc": "23155-862-03", "marketing_start_date": "20240221"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-862-05)", "package_ndc": "23155-862-05", "marketing_start_date": "20240221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (23155-862-09)", "package_ndc": "23155-862-09", "marketing_start_date": "20240221"}], "brand_name": "Modafinil", "product_id": "23155-862_d8fc4961-6cbc-44fc-be5f-63127fff98f8", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic-like Agent [EPC]"], "product_ndc": "23155-862", "dea_schedule": "CIV", "generic_name": "Modafinil", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Modafinil", "active_ingredients": [{"name": "MODAFINIL", "strength": "200 mg/1"}], "application_number": "ANDA207196", "marketing_category": "ANDA", "marketing_start_date": "20240221", "listing_expiration_date": "20261231"}