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The FDA has recalled a batch of finasteride made by one pharmacy. Here's what's going on—and how to know if your finasteride is safe to take.
DATE OF RECALL: March 2, 2023. DRUG NAME: Multiple Products distributed. RECALLING FIRM: Accord Healthcare, Inc. REASON FOR RECALL: This recall was issued due to CGMP Deviations following an FDA inspection. FDA LINK: N/A.
The last Recall Enforcement Report for Finasteride with NDC 16729-089 was initiated on 02-07-2023 as a Class II recall and it is currently terminated.
MasterPharm, LLC. is voluntarily recalling 1 lot of Finasteride Plus 1.25mg, capsules to the consumer level. The Finasteride Plus capsules have been found to contain undeclared minoxidil, an...
The trials demonstrated an overall reduction in prostate cancer diagnoses with finasteride 5 mg and dutasteride treatment (see Data Summary below). This overall reduction was due to a decreased...
10/16/2024. FDA provides a searchable list of recalled products. Drug recalls are actions taken by a firm to remove a product from the market and may be conducted on a firm's own initiative, by...
March 28: Greenstone Announces Voluntary Nationwide Recall of Citalopram and Finasteride Due to Possible Mislabeling. This includes Citalopram 10mg Tablets (100-count bottle) and Finasteride 5mg Tablets (90-count bottle), both distributed in the U.S. market.
MasterPharm recalled one lot of Finasteride Plus, a hair loss drug that comes in capsules. It has too much minoxidil, which isn’t named in the ingredients. Heart failure or heart damage can...
The recall is due to the possibility that a third-party manufacturer has placed incorrect labels on the bottles; specifically, bottles that are labeled as citalopram lot number FI0510058-A may contain finasteride, which is indicated for treatment of BPH.
MasterPharm, LLC, is voluntarily recalling 1 lot of Finasteride Plus 1.25mg sold in orange prescription bottles containing 30 capsules or blue prescription bottles containing 90 capsules.