Finasteride Tablets recall
Finasteride Tablets, USP 5 mg, 90-count bottles, Rx only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs…
Why was Finasteride Tablets recalled?
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: FIN16002, Exp. 03/2018
- Product
- Finasteride Tablets, USP 5 mg, 90-count bottles, Rx only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs…
- Recalling firm
- Hetero Drugs Ltd. - Unit 1
- Quantity
- 20,412 units
- Distribution
- NJ only.
- Recall date
- February 8, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)