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
Reported: February 8, 2017 Initiated: December 29, 2016 #D-0453-2017
Product Description
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.
Details
- Recalling Firm
- Hetero Drugs Ltd. - Unit 1
- Units Affected
- 20,412 units
- Distribution
- NJ only.
- Location
- Medak District, N/A
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Hetero Drugs Ltd. - Unit 1. Units affected: 20,412 units.
Why was this product recalled? ▼
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 8, 2017. Severity: Low. Recall number: D-0453-2017.
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