RecallRadar

FDA Drug recall D-0816-2016

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 100 ct. bottle, Rx O…

On 2016-04-13 the FDA classified a Class II recall of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 100 ct. bottle, Rx O… by Actavis Elizabeth, citing failed Impurities/Degradation Specifications: Out of specification for impurities.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0816-2016
ClassificationClass II
Statusterminated
Initiated2016-02-16
Published2016-04-13
Last updated2026-09-13 11:51 UTC
CompanyActavis Elizabeth
DistributionUS

Product

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, Morristown, NJ 07960. NDC: 45963-743-11.

Reason

Failed Impurities/Degradation Specifications: Out of specification for impurities.

Identifiers

code_infoLot #: 5245M141, Expiry: 6/16; Lot #: 0953C151, Expiry date: 8/16Lot #: 1728D151, Expiry: 9/16; Lot #: 3205G152, Expiry: 3/17.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0816-2016%22

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