FDA.reportPublic FDA data

NoDoz Alertness Aid

Product NDC
66715-9799
Requested package NDC
66715-9799-2
11-digit product format
667159799
Labeler code
66715
Product ID
66715-9799_dd1d722d-1aca-a249-e053-2995a90a7333
Type
HUMAN OTC DRUG
Nonproprietary name
Caffeine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lil' Drug Store Products, Inc.
Application
part340
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-12-07
Marketing end
0000-00-00
Substance
CAFFEINE
Active strength
200 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage66715-979966715-9799-2DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDCRelated label
66715-9799-0NoDoz® Alertness Aid Maximum Strength
66715-9799-2NoDoz® Alertness Aid Maximum Strength
66715-9799-3NoDoz® Alertness Aid Maximum Strength
66715-9799-4NoDoz® Alertness Aid Maximum Strength
66715-9799-6NoDoz® Alertness Aid Maximum Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66715-9799-0NoDoz Alertness AidMaximum Strength10 in 1 VIAL, PLASTICTABLET, FILM COATED106
66715-9799-2NoDoz Alertness AidMaximum Strength2 in 1 POUCHTABLET, FILM COATED26
66715-9799-2NoDoz Alertness AidMaximum Strength2 in 1 CARTONTABLET, FILM COATED26
66715-9799-3NoDoz Alertness AidMaximum Strength3 in 1 CARTONTABLET, FILM COATED36
66715-9799-3NoDoz Alertness AidMaximum Strength2 in 1 POUCHTABLET, FILM COATED26
66715-9799-4NoDoz Alertness AidMaximum Strength10 in 1 BLISTER PACKTABLET, FILM COATED106
66715-9799-4NoDoz Alertness AidMaximum Strength2 in 1 CARTONTABLET, FILM COATED26
66715-9799-6NoDoz Alertness AidMaximum Strength1 in 1 CARTONTABLET, FILM COATED16
66715-9799-6NoDoz Alertness AidMaximum Strength60 in 1 BOTTLE, PLASTICTABLET, FILM COATED606

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66715-9799NODOZ ALERTNESS AID MAXIMUM STRENGTH (CAFFEINE) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC.]6Legacy NDC, 9 package rows20220731_54d47b7a-66a1-4f86-b478-f2f8737cd030.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198520caffeine 200 MG Oral TabletPSN54d47b7a-66a1-4f86-b478-f2f8737cd0306
795925NoDoz 200 MG Oral TabletPSN54d47b7a-66a1-4f86-b478-f2f8737cd0306
795925caffeine 200 MG Oral Tablet [No Doz]SBD54d47b7a-66a1-4f86-b478-f2f8737cd0306
198520caffeine 200 MG Oral TabletSCD54d47b7a-66a1-4f86-b478-f2f8737cd0306
795925No Doz 200 MG Oral TabletSY54d47b7a-66a1-4f86-b478-f2f8737cd0306

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66715-9799-2667159799022 POUCH in 1 CARTON (66715-9799-2) > 2 TABLET, FILM COATED in 1 POUCH2 pouch2018-06-012023-12-30NoNoCurrent