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05/13/2024
Louisiana legislators are considering classifying abortion-inducing drugs as controlled substances, potentially restricting access, criminalizing the use of the medication outside of a prescription, and impacting medical care beyond abortion.
Louisiana legislators are considering classifying abortion-inducing drugs as controlled substances, potentially restricting access, criminalizing the use of the medication outside of a prescription, and impacting medical care beyond abortion.
Louisiana legislators are...
05/13/2024
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05/09/2024
Imprimis NJOF is recalling 3320 bottles of compounded prednisolone sodium phosphate 1%, moxifloxacin 0.5%, and bromfenac 0.075% ophthalmic solution due to being subpotent.
Imprimis NJOF is recalling 3320 bottles of compounded prednisolone sodium phosphate 1%, moxifloxacin 0.5%, and bromfenac 0.075% ophthalmic solution due to being subpotent.
Imprimis NJOF is recalling 3320...
05/09/2024
Pharmacy Learning Network
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05/09/2024
Amneal Pharmaceuticals of New York is recalling 2784 bottles of methylergonovine maleate tablets because they are subpotent.
Amneal Pharmaceuticals of New York is recalling 2784 bottles of methylergonovine maleate tablets because they are subpotent.
Amneal Pharmaceuticals of New...
05/09/2024
Pharmacy Learning Network
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05/09/2024
Two lots of compounded epinephrine 0.025% and lidocaine HCl 0.75% intraocular solution for injection are being recalled by Imprimis NJOF. The May 8, 2024, US Food and Drug Administration (FDA) Enforcement Report states the solution is “out of...
Two lots of compounded epinephrine 0.025% and lidocaine HCl 0.75% intraocular solution for injection are being recalled by Imprimis NJOF. The May 8, 2024, US Food and Drug Administration (FDA) Enforcement Report states the solution is “out of...
Two lots of compounded...
05/09/2024
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05/02/2024
Cipla USA Inc. is recalling two lots of ipratropium bromide and albuterol sulfate inhalation solution.
Cipla USA Inc. is recalling two lots of ipratropium bromide and albuterol sulfate inhalation solution.
Cipla USA Inc. is recalling two...
05/02/2024
Pharmacy Learning Network
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05/02/2024
Nomax Inc. is recalling more than 42,000 cartons of GloStrips and Ful-Glo fluorescein sodium ophthalmic strips because the active pharmaceutical ingredient used in the products failed to meet impurity specifications.
Nomax Inc. is recalling more than 42,000 cartons of GloStrips and Ful-Glo fluorescein sodium ophthalmic strips because the active pharmaceutical ingredient used in the products failed to meet impurity specifications.
Nomax Inc. is recalling more...
05/02/2024
Pharmacy Learning Network
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05/01/2024
More than 40 lots of Aruba Aloe Hand Sanitizer Gel and Aruba Aloe Alcoholada Gel are under a Class I recall because they have been found to contain alcohol denatured with methanol.
More than 40 lots of Aruba Aloe Hand Sanitizer Gel and Aruba Aloe Alcoholada Gel are under a Class I recall because they have been found to contain alcohol denatured with methanol.
More than 40 lots of Aruba Aloe...
05/01/2024
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04/26/2024
The FDA proposed introducing a Patient Medication Information (PMI), in addition to the Medication Guide, to provide clear and concise details about prescription medications to improve patient understanding and adherence, ultimately reducing...
The FDA proposed introducing a Patient Medication Information (PMI), in addition to the Medication Guide, to provide clear and concise details about prescription medications to improve patient understanding and adherence, ultimately reducing...
The FDA proposed introducing a...
04/26/2024
Pharmacy Learning Network
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04/24/2024
Lupin Pharmaceuticals Inc. is recalling 26,352 bottles of rifampin capsules because the drug is subpotent, according to the April 17, 2024, US Food and Drug Administration (FDA) Enforcement Report.
Lupin Pharmaceuticals Inc. is recalling 26,352 bottles of rifampin capsules because the drug is subpotent, according to the April 17, 2024, US Food and Drug Administration (FDA) Enforcement Report.
Lupin Pharmaceuticals Inc. is...
04/24/2024
Pharmacy Learning Network
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04/24/2024
Teva Pharmaceuticals USA Inc. is recalling a single lot of isotretinoin capsules over concerns of superpotency. According to the April 17, 2024, US Food and Drug Administration (FDA) Enforcement Report, results from 3-month stability testing...
Teva Pharmaceuticals USA Inc. is recalling a single lot of isotretinoin capsules over concerns of superpotency. According to the April 17, 2024, US Food and Drug Administration (FDA) Enforcement Report, results from 3-month stability testing...
Teva Pharmaceuticals USA Inc. is...
04/24/2024
Pharmacy Learning Network

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