CIALIS (Tadalafil) Tablet, Film Coated [Unit Dose Services]
Updated Date: Nov 14, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 14, 2018 Category: Drugs & Pharmacology Source Type: alerts

TADALAFIL Tablet, Film Coated [AvKARE, Inc.]
Updated Date: Oct 17, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 17, 2018 Category: Drugs & Pharmacology Source Type: alerts

TADALAFIL Tablet, Film Coated [Prasco Laboratories ]
Updated Date: Sep 28, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 28, 2018 Category: Drugs & Pharmacology Source Type: alerts

TADALAFIL Tablet, Film Coated [Teva Pharmaceuticals USA, Inc.]
Updated Date: Sep 27, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 27, 2018 Category: Drugs & Pharmacology Source Type: alerts

TADALAFIL Tablet, Film Coated [Mylan Pharmaceuticals Inc.]
Updated Date: Aug 13, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - August 13, 2018 Category: Drugs & Pharmacology Source Type: alerts

AX PHARMACEUTICAL CORP (Tadalafil) Powder [AX Pharmaceutical Corp]
Updated Date: May 2, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 2, 2018 Category: Drugs & Pharmacology Source Type: alerts

Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil
Overland Park, KS, Epic Products, LLC is voluntarily recalling all lots of Euphoric capsules, packaged in 1 count blister cards, 3 count bottles, and 12 count bottles to the consumer level. FDA analysis found samples of Euphoric to be tainted with undeclared sildenafil and tadalafil, active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterase 5-inhibitors (PDE-5 inhibitors), used to treat male erectile dysfunction (ED). The presence of sildenafil and tadalafil in Euphoric renders it an unapproved drug for which safety and efficacy have not been established and, therefore subject to re...
Source: FDA Health Fraud Alerts - April 17, 2018 Category: Medical Law Source Type: alerts

ADCIRCA (Tadalafil) Tablet [Aphena Pharma Solutions - Tennessee, LLC]
Updated Date: Oct 18, 2017 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 18, 2017 Category: Drugs & Pharmacology Source Type: alerts

AX PHARMACEUTICAL CORP (Tadalafil) Powder [AX Pharmaceutical Corp]
Updated Date: Aug 24, 2017 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - August 24, 2017 Category: Drugs & Pharmacology Source Type: alerts

ADCIRCA (Tadalafil) Tablet [Avera McKennan Hospital]
Updated Date: Apr 12, 2017 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - April 12, 2017 Category: Drugs & Pharmacology Source Type: alerts

A & H Focal Inc. Issues Nationwide Recall of 21 Products Marketed as Dietary Supplements & One Cosmetic Product Due to the Possible Presence of Undeclared Erectile Dysfunction Ingredients
A&H Focal Inc. is voluntarily recalling all lots of the following products because many of these products have been historically tested by the FDA and found to contain PDE-5 Inhibitors (i.e. sildenafil, tadalafil, vardenafil, etc.) which is the active ingredient in an FDA-approved drug for erectile dysfunction (ED) making these tainted dietary supplements unapproved drugs. (Source: FDA Health Fraud Alerts)
Source: FDA Health Fraud Alerts - March 7, 2017 Category: Medical Law Source Type: alerts

Organic Herbal Supply, Inc. Announces a Voluntary Nationwide Recall of XtraHRD Natural Male Enhancement Capsules
Organic Herbal Supply, Inc. announced today that it is conducting a voluntary nationwide recall of all lots of XtraHRD Natural Male Enhancement capsules. FDA analysis has found the product to contain Tadalafil. Tadalafil is a FDA-approved drug used as treatment for male Erectile Dysfunction (ED). The active drug ingredients are not listed on the label for this product. To date, no adverse events have been reported. (Source: FDA Health Fraud Alerts)
Source: FDA Health Fraud Alerts - February 21, 2017 Category: Medical Law Source Type: alerts