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FDA Approves New Treatment Option for Patients with ALS
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474
FDA
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Golden State Medical Supply, Inc. Issues a Voluntary Nationwide Recall of Atenolol 25 mg Tablets and Clopidogrel 75 mg Tablets Due to a Label Mix-up
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473
FDA
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Radioactive Drug Research Committee (RDRC) Program
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586
FDA
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BEST Resource Taxonomy
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508
FDA
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FDA Continues Important Work on Substance Use and Overdose Prevention Efforts
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488
FDA
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Proper Trade LLC/My Stellar Lifestyle Issues Voluntary Nationwide Recall of Wonder Pill Capsules Due to the Presence of Undeclared Tadalafil
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521
FDA
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Guidance for Industry: Color Additive Petitions - FDA Recommendations for Submission of Chemical and Technological Data on Color Additives for Food, D
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444
FDA
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Providing Over-the-Counter Monograph Submissions in Electronic Format
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507
FDA
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System Kosmetik Produktionsgesellschaft fur kosmetische Gmbh - 632727 - 09/09/2022
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436
FDA
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Muscle Sports Products, LLC - 625731 - 09/23/2022
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476
FDA
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Zhejiang Tianyu Pharmaceutical Co., Ltd. - 631054 - 08/17/2022
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534
FDA
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Eugia US LLC Issues Voluntary Nationwide Recall of Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), Due to the Presence of Particulate Matter
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444
FDA
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New co-chairs elected for working parties for healthcare professionals and for patients and consumers, , 23/09/2022
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513
EMA
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FDA Issues New Guidance to Help Facilitate Availability of Naloxone to Prevent Opioid Overdoses and Reduce Death
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463
FDA
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Ethical Considerations for Clinical Investigations of Medical Products Involving Children
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467
FDA
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Data Standards Catalog v8.2
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424
FDA
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Guidance Recap Podcast | Ethical Considerations for Clinical Investigations of Medical Products Involving Children
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451
FDA
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RXQ Compounding, LLC Issues Voluntary Nationwide Recall of All Sterile Products within Expiry and Voluntarily Cessation of Production Due to the Lack
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520
FDA
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Precision Dose Inc. Issues Voluntary Nationwide Recall of Ranitidine Oral Solution, USP 150 mg/10 mL Due to Possible Presence of N-nitrosodimethylamin
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517
FDA
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Information about Naloxone
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468
FDA
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