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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

Drug Recall

Official source record

Recall number
D-0453-2017
Event ID
76120
Classification
Class III
Status
Terminated
Recalling company
Hetero Drugs Ltd. - Unit 1
Reason for recall
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
Report date
February 8, 2017
Recall initiation date
December 29, 2016
Termination date
July 11, 2017
Distribution pattern
NJ only.

Drug product identifiers

Manufacturer
Camber Pharmaceuticals, Inc.
Brand name
FINASTERIDE
Generic name
FINASTERIDE
Substance name
FINASTERIDE
Product NDC
31722-525
Package NDCs
31722-525-01; 31722-525-05; 31722-525-10; 31722-525-30; 31722-525-90
Route
ORAL

Where this information comes from

View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this medication?

Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.

Where can I find more official information?

The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.