Teva is voluntarily recalling a single lot of Anagrelide Capsules, USP 0.5mg, due to dissolution failure that was detected during a routine stability test. Teva is voluntarily recalling a single lot ...

Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary ...

Ill-dissolving capsules can hamper drugs’ effectiveness or render them useless, which is especially concerning when they’re used to treat seriously sick blood disorder patients. Teva Pharmaceuticals ...

ATLANTA — Several lots of an ADHD medication has been recalled over concerns revealed by testing. Sun Pharmaceutical Industries Inc. has initiated a voluntary recall of Lisdexamfetamine Dimesylate ...

A popular ADHD medication is facing a nationwide recall because tests suggest users will not benefit from the full effect of the drug. The Food and Drug Administration reported on October 28 that ...

SAN DIEGO, March 9, 2023 /PRNewswire/ -- Neurocrine Biosciences, Inc. (Nasdaq: NBIX) today announced it will present data from three in vitro dissolution studies exploring the dissolution performance ...

WASHINGTON — Several lots of a prescription ADHD medication have been recalled due to some failed lab tests, according to FDA Enforcement Reports. The nationwide recall covers several batches of the ...