FDA recall record

Zydus Pharmaceuticals USA BENZONATATE Capsules, USP, 200 mg, 100 Capsule Bottles recall — FDA D-0289-2015

Presence of Foreign Capsules/Tablets: Benzonatate 100 mg co-mingled with benzonatate 200 mg capsules.

Class IIIclassification
D-0289-2015official record ID
Dec 10, 2014report date

Recall record at a glance

Official recordD-0289-2015
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmZydus Pharmaceuticals USA Inc.
Report dateDec 10, 2014
Recall initiation dateSep 24, 2014
Quantity63,648 Bottles
LocationPennington, NJ, United States

Official product description

BENZONATATE Capsules, USP, 200 mg, 100 Capsule Bottles, Rx only. Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA, Inc. NDC: 68382-248-01

Why the product was recalled

Presence of Foreign Capsules/Tablets: Benzonatate 100 mg co-mingled with benzonatate 200 mg capsules.

Distribution information

US Nationwide including Puerto Rico

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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