Finasteride Tablets, USP 5 mg, 90-count bottles, Rx only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs, Unit V Polepally, Jadcheria, Mahaboob Nagar - 509 301, India Limited NDC 31722-525-90

FDA recall notice · announced February 8, 2017 · Hetero Drugs Ltd. - Unit 1

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

Finasteride Tablets, USP 5 mg, 90-count bottles, Rx only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs, Unit V Polepally, Jadcheria, Mahaboob Nagar - 509 301, India Limited NDC 31722-525-90

Reason for recall

Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.

Notes

Distribution: NJ only.
Lot/code information: Lot #: FIN16002, Exp. 03/2018
Quantity: 20,412 units
Status: Terminated
Products in this recall event:
- Finasteride Tablets, USP 5 mg, 90-count bottles, Rx only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs, Unit V Polepally, Jadcheria, Mahaboob Nagar - 509 (D-0453-2017)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.