What's New on the FDA Drugs Site
June 15, 2017
- CDER Statement: FDA updates on Pfizer drug shortages
- Notice to Industry: With End of Pilot Project, FDA Introduces Updated Form To Submit Field Alert Reports (FARs) Electronically
- Report a Product Quality Issue—The purpose of field alert reports (FARs) is to quickly identify quality defects in distributed drug products that may present a potential safety threat.
- Drug Firm Annual Registration Status (updated)
- Drug Firm Annual Registration Status Download File (updated)
- Medication Guides Page (Updated)
- National Drug Code Directory
- Statement from FDA Commissioner Scott Gottlieb, M.D. – FDA is taking new steps to help assess opioid drugs with abuse-deterrent properties
- Teva Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One Lot of Paliperidone Extended-Release Tablets, 3mg, 90 Count Bottles Distributed Under the Actavis Pharma Inc. Label Due to Dissolution Test Failure
- Topical Products by Phillips Company: Recall - Due to Concerns of Manufacturing Practices
- Wholesale Distributor and Third-Party Logistics Providers Reporting (updated)
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