Info Obat dan Regulator Obat Dunia

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Bryant Ranch Prepack Inc. Issues Voluntary Nationwide Recall of Morphine Sulfate 30 mg Extended Release and Morphine Sulfate 60 mg Extended-Release Du
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259
FDA
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FDA warns about possible increased risk of death and serious side effects with cancer drug Copiktra (duvelisib)
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247
FDA
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Generic Drugs Program Activities Report - Monthly Performance
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268
FDA
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Copiktra (duvelisib): Drug Safety Communication - FDA Warns about Possible Increased Risk of Death and Serious Side Effects
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259
FDA
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Patient-Focused Drug Development: Selecting, Developing, or Modifying Fit-for-Purpose Clinical Outcome Assessments
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297
FDA
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Loud Muscle Science, LLC Issues Voluntary Recall of Launch Sequence Capsules Due to the Presence of Undeclared Tadalafil in United States and Canada
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318
FDA
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Monkeypox: EMA starts review for Imvanex, CHMP, 28/06/2022
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297
EMA
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Call for companies to register their Industry Single Point of Contact (i-SPOC) on supply and availability, , 28/06/2022
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244
EMA
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DLG Naturals, Inc. - 622277 - 04/28/2022
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285
FDA
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Fagron Group B.V. - 624255 - 06/14/2022
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249
FDA
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Mirfeel Korea Co., Ltd. - 627401 - 06/22/2022
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300
FDA
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Industrias Cklass S. de R.L. de C.V. - 610275 - 06/22/2022
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281
FDA
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Golden Lab LLC - 625783 - 05/26/2022
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249
FDA
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Monarch PCM, LLC - 620779 - 06/10/2022
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294
FDA
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FDA approves treatment for chronic weight management in pediatric patients aged 12 years and older
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288
FDA
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FDA approves lisocabtagene maraleucel for second-line treatment of large B-cell lymphoma
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274
FDA
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The FDA Announces Proposed Rule: Nonprescription Drug Product with an Additional Condition for Nonprescription Use
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270
FDA
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Drug Safety Oversight Board Meetings - Public Summaries
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251
FDA
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Over-the-Counter OTC | Nonprescription Drugs
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342
FDA
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An FDA Self-Audit of Continuous Manufacturing for Drug Products | Audio Transcript
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240
FDA
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