Tag: pharmaceutical quality control

Import Alerts: How the FDA Blocks Drugs from Non-Compliant Manufacturers

Import Alerts: How the FDA Blocks Drugs from Non-Compliant Manufacturers
wayne Holloway in: Medications 20 December 2025

The FDA uses Import Alerts to block drugs from non-compliant manufacturers, automatically detaining shipments without inspection. Learn how the Green List works, why Indian and Chinese suppliers are being targeted, and what manufacturers must do to stay in the U.S. market.

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NSAIDs and Peptic Ulcer Disease: Understanding the Real Risk of Gastrointestinal Bleeding
NSAIDs and Peptic Ulcer Disease: Understanding the Real Risk of Gastrointestinal Bleeding

NSAIDs like ibuprofen and naproxen are common pain relievers, but they can cause serious stomach bleeding, especially in older adults or those with risk factors. Learn who’s most at risk, how to protect yourself, and what alternatives exist.

Published ON: 2 Dec
Antihistamines: First-Generation vs. Second-Generation Compared
Antihistamines: First-Generation vs. Second-Generation Compared

First-generation antihistamines like Benadryl work fast but cause drowsiness. Second-generation options like Zyrtec and Claritin are non-sedating and better for daily use. Learn which is right for your allergies.

Published ON: 3 Dec
Lithium Carbonate Generics: What You Need to Know About Serum Levels
Lithium Carbonate Generics: What You Need to Know About Serum Levels

Lithium carbonate generics require strict serum level monitoring due to their narrow therapeutic index. Learn how brand switches, dosing, age, and kidney function affect safety and effectiveness in bipolar disorder treatment.

Published ON: 12 Dec
Prescriber Override: When Doctors Can Require Brand-Name Drugs Instead of Generics
Prescriber Override: When Doctors Can Require Brand-Name Drugs Instead of Generics

Prescriber override lets doctors require brand-name drugs instead of generics when safety is at risk. Learn how DAW-1 codes work, state-by-state rules, and when overrides are necessary-or dangerous.

Published ON: 15 Dec
FDA Warning Authority: How the Agency Takes Action Against Non-Compliant Manufacturers
FDA Warning Authority: How the Agency Takes Action Against Non-Compliant Manufacturers

The FDA issues warning letters to manufacturers who violate safety and labeling laws. These letters are the first step in enforcement that can lead to recalls, fines, or criminal charges. Learn how the agency targets non-compliant companies and what you must do to avoid serious consequences.

Published ON: 1 Dec

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