Drugplain

Alert 200 mg/1

Caffeine · TABLET, FILM COATED · Time Cap Labs, Inc

5 Recalls on Record
Plain English

Alert is a tablet, film coated containing caffeine at 200 mg/1, taken oral. Manufactured by Time Cap Labs, Inc.

Key Facts

Brand Name
Alert
Generic Name
Caffeine
NDC Code (Product)
49483-343
Manufacturer
Time Cap Labs, Inc
Strength
200 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
part340
Drug Class
Central Nervous System Stimulant [EPC]; Methylxanthine [EPC]
Marketing Start
11/30/2011

Recall History

5 Recalls on Record
Class III09/20/2022

QuVa Pharma, Inc.

Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of 0.45% Sodium Chloride (500mL) instead of 0.9% Sodium Chloride (500mL).

TerminatedVoluntary: Firm initiated
Class III12/16/2019

Pharmedium Services, LLC

Subpotent Drug

TerminatedVoluntary: Firm initiated
Class III12/16/2019

Pharmedium Services, LLC

Subpotent Drug

TerminatedVoluntary: Firm initiated
Class II06/23/2022

Family Dollar Stores, Llc.

CGMP Deviations: product held outside appropriate storage temperature conditions.

OngoingVoluntary: Firm initiated
Class III12/16/2019

Pharmedium Services, LLC

Subpotent Drug

TerminatedVoluntary: Firm initiated

Frequently Asked Questions

What is Alert used for?

Alert contains Caffeine. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Alert a controlled substance?

Alert is not classified as a controlled substance by the DEA.

What is the generic name for Alert?

The generic name for Alert is Caffeine. There are 12 other brand versions of Caffeine.

What is the NDC code for Alert 200 mg/1?

The NDC (National Drug Code) for Alert 200 mg/1 is 49483-343, listed by Time Cap Labs, Inc.